opmi lumera 700 - zeiss

OPMI LUMERA 700Software Release 3.1

Instructions for Use

Copyright

© 2018, Carl Zeiss Meditec AG, Jena

Brand names/Trademarks

CALLISTO eye, Invertertube, HaMode, K TRACK, MEDIALINK,OPMI LUMERA, RESIGHT, SCI, Superlux, VISULUX, Visionguard andZ ALIGN are either trademarks or registered trademarks of CarlZeiss Meditec AG or other companies of the ZEISS Group inGermany and/or other countries.

All other trademarks mentioned in this document are the propertyof their respective owners.

Instructions for Use Table of contentsOPMI LUMERA 700

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Table of contents

1 Notes on Instructions for Use..................................................................... 11

1.1 Device name ....................................................................................................................... 11

1.2 Area of application ............................................................................................................. 11

1.3 Purpose and storage of the documentation ....................................................................... 11

1.4 Questions and comments ................................................................................................... 11

1.5 Conventions in this document ............................................................................................ 111.5.1 Conventions in all text areas............................................................................................................ 111.5.2 Conventions in a course of action.................................................................................................... 12

1.6 Other applicable documents ............................................................................................... 13

2 Safety notes ............................................................................................... 15

2.1 Target group ...................................................................................................................... 15

2.2 Area of use ......................................................................................................................... 152.2.1 Intended use ................................................................................................................................... 152.2.2 Normal use...................................................................................................................................... 15

2.3 Responsibilities and duties of the operator ........................................................................ 162.3.1 Messages to manufacturer and authorities ...................................................................................... 17

2.4 Measures and duties of the operator.................................................................................. 18

2.5 Electromagnetic compatibility ............................................................................................ 19

2.6 Requirements for operation................................................................................................ 192.6.1 Before commissioning for the first time ........................................................................................... 192.6.2 Before every use.............................................................................................................................. 202.6.3 During operation............................................................................................................................. 222.6.4 After every use ................................................................................................................................ 23

2.7 Measures to prevent phototoxic injury ............................................................................... 242.7.1 Illumination characteristics (spectral composition)............................................................................ 242.7.2 Illumination intensity ....................................................................................................................... 242.7.3 Angle of illumination ....................................................................................................................... 252.7.4 Focus of the light source ................................................................................................................. 252.7.5 Exposure time to light ..................................................................................................................... 25

2.8 Maximum radiation exposure............................................................................................. 272.8.1 Maximum radiation exposure times with red reflex illumination ...................................................... 272.8.2 Maximum radiation exposure times with surrounding field illumination........................................... 282.8.3 Maximum radiation exposure times with integrated slit illuminator ................................................. 282.8.4 References ...................................................................................................................................... 28

3 Description of the device............................................................................ 31

3.1 Device marking................................................................................................................... 31

3.2 Device setup ....................................................................................................................... 353.2.1 CALLISTO eye Panel PC.................................................................................................................... 363.2.2 Support arm for CALLISTO eye Panel PC .......................................................................................... 363.2.3 Lamp housing ................................................................................................................................. 37

Table of contents Instructions for UseOPMI LUMERA 700

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3.2.4 Suspension arm............................................................................................................................... 393.2.5 XY coupling..................................................................................................................................... 393.2.6 Overhead display............................................................................................................................. 403.2.7 Surgical microscope......................................................................................................................... 403.2.8 Assistant's microscope .................................................................................................................... 423.2.9 14-function foot control panel ........................................................................................................ 433.2.10 Stand base ...................................................................................................................................... 433.2.11 Stand column.................................................................................................................................. 443.2.12 Support arm with connector panel .................................................................................................. 443.2.13 Integrated 22" monitor ................................................................................................................... 453.2.14 Support arm for integrated 22" monitor.......................................................................................... 453.2.15 Instrument tray................................................................................................................................ 463.2.16 Integrated keratoscope ring ............................................................................................................ 463.2.17 Connections on the surgical microscope.......................................................................................... 473.2.18 Connections on the assistant's microscope...................................................................................... 473.2.19 Connector panel.............................................................................................................................. 483.2.20 Connector panel for the integrated HD camera ............................................................................... 483.2.21 CALLISTO eye Panel PC connector panel (model I) ........................................................................... 493.2.22 CALLISTO eye Panel PC connector panel (model II) .......................................................................... 49

3.3 Control elements and displays ............................................................................................ 503.3.1 Superlux Eye light source fault signal ............................................................................................... 503.3.2 Halogen light source fault signal...................................................................................................... 513.3.3 LED light source fault signal............................................................................................................. 513.3.4 Manual mode fault signal ................................................................................................................ 523.3.5 Overhead display............................................................................................................................. 533.3.6 Surgical microscope......................................................................................................................... 543.3.7 Assistant's microscope .................................................................................................................... 553.3.8 Invertertube E.................................................................................................................................. 563.3.9 Widefield eyepiece .......................................................................................................................... 573.3.10 Handgrips........................................................................................................................................ 573.3.11 14-function foot control panel ........................................................................................................ 583.3.12 XY coupling..................................................................................................................................... 593.3.13 Suspension arm............................................................................................................................... 603.3.14 Control panel .................................................................................................................................. 613.3.15 CALLISTO eye Panel PC (model I) ..................................................................................................... 623.3.16 CALLISTO eye Panel PC (model II) .................................................................................................... 633.3.17 Superlux Eye light source................................................................................................................. 643.3.18 Halogen light source ....................................................................................................................... 64

3.4 Software description .......................................................................................................... 653.4.1 Structure of the operating panel...................................................................................................... 653.4.2 Bottom bar...................................................................................................................................... 653.4.3 Status bar........................................................................................................................................ 663.4.4 Color code ...................................................................................................................................... 673.4.5 Interactive buttons .......................................................................................................................... 673.4.6 Navigation buttons.......................................................................................................................... 693.4.7 Control panel keyboard ................................................................................................................... 703.4.8 Settings for daily operation - main menu, tab 1 ............................................................................... 713.4.9 Basic device settings - main menu, tab 2 ......................................................................................... 723.4.10 Factory settings for handgrips and 14-function foot control panel................................................... 733.4.11 Configurable assignments for handgrips and the 14-function foot control panel ............................. 76

3.5 Functional description ........................................................................................................ 793.5.1 Operating concept .......................................................................................................................... 793.5.2 SCI illumination ............................................................................................................................... 81


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3.5.3 Main and auxiliary light source ........................................................................................................ 813.5.4 Total magnification ......................................................................................................................... 823.5.5 Fast focus........................................................................................................................................ 823.5.6 RESIGHT functions........................................................................................................................... 833.5.7 DeepView ....................................................................................................................................... 833.5.8 Reset options .................................................................................................................................. 833.5.9 Links................................................................................................................................................ 843.5.10 Manual mode.................................................................................................................................. 843.5.11 Assistant's microscope .................................................................................................................... 853.5.12 IDIS (Integrated Data Injection System)............................................................................................ 853.5.13 Integrated slit illumination ............................................................................................................... 863.5.14 Integrated HD camera ..................................................................................................................... 863.5.15 Integrated HD video and image recording ....................................................................................... 87

4 Installation ................................................................................................. 89

4.1 Safety during installation.................................................................................................... 89

4.2 Preparing the installation ................................................................................................... 904.2.1 Requirements for connecting the device to an IT network ............................................................... 90

4.3 Connections........................................................................................................................ 924.3.1 Connecting the power supply.......................................................................................................... 924.3.2 Connecting the 14-function foot control panel................................................................................ 934.3.3 Setting up a network connection with the CALLISTO eye Panel PC .................................................. 944.3.4 Setting up a network connection with integrated CALLISTO eye Panel PC ....................................... 984.3.5 Connecting IDIS via CALLISTO eye Panel PC................................................................................... 1004.3.6 Connecting external video devices................................................................................................. 1024.3.7 Connecting the strain relief ........................................................................................................... 104

5 Daily startup............................................................................................. 105

5.1 Outfitting the surgical and assistant's microscopes with accessories ............................... 1055.1.1 Replacing accessories and components ......................................................................................... 1055.1.2 Connecting the Invertertube E ....................................................................................................... 1085.1.3 Connecting RESIGHT 700 .............................................................................................................. 1105.1.4 Connecting auxiliary illumination ................................................................................................... 1105.1.5 Balancing the system..................................................................................................................... 111

5.2 Adjusting the surgical and assistant's microscopes .......................................................... 1135.2.1 Adjusting the downward travel limit.............................................................................................. 1135.2.2 Adjusting friction........................................................................................................................... 1145.2.3 Positioning the assistant's microscope ........................................................................................... 1145.2.4 Adjusting microscope tilt ............................................................................................................... 1155.2.5 Adjusting the tubes and eyepieces................................................................................................. 1165.2.6 Adjusting the working distance and magnification ........................................................................ 117

5.3 Positioning the device in the OR....................................................................................... 1185.3.1 Moving the device......................................................................................................................... 1185.3.2 Swiveling the device over the surgical field .................................................................................... 1195.3.3 Placing the device in the working position..................................................................................... 1205.3.4 Orienting the integrated CALLISTO eye Panel PC ........................................................................... 1215.3.5 Orienting the integrated 22" monitor ............................................................................................ 122

6 Before every use....................................................................................... 123


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6.1 Safety during preparation................................................................................................. 123

6.2 Switching the device on ................................................................................................... 124

6.3 Function test .................................................................................................................... 1256.3.1 Device function tests ..................................................................................................................... 1256.3.2 Function tests for device with fundus viewing system.................................................................... 126

6.4 Preparing the system for sterile use ................................................................................. 1276.4.1 Attaching sterile accessories .......................................................................................................... 1276.4.2 Placing the drape .......................................................................................................................... 129

7 Operation................................................................................................. 131

7.1 Safety during operation.................................................................................................... 131

7.2 Configuring user and surgery profiles............................................................................... 1327.2.1 Creating and activating users......................................................................................................... 1327.2.2 Changing the user language.......................................................................................................... 1337.2.3 Deleting users ............................................................................................................................... 1337.2.4 Creating a "Cataract" surgery profile ............................................................................................. 1337.2.5 Creating a "Retina RESIGHT" surgery profile .................................................................................. 1347.2.6 Creating a "Retina Contact" surgery profile ................................................................................... 1357.2.7 Assigning the RESIGHT function to the surgery profile ................................................................... 1367.2.8 Configuring working steps ............................................................................................................ 1377.2.9 Deleting a surgery profile .............................................................................................................. 138

7.3 Device-specific software configuration............................................................................. 1387.3.1 Setting the date and time.............................................................................................................. 1387.3.2 Configuring optics ......................................................................................................................... 1397.3.3 Pairing........................................................................................................................................... 1407.3.4 Configuring the video signal of the integrated HD camera............................................................. 1417.3.5 Configuring the network connection with CALLISTO eye ............................................................... 1427.3.6 Configuring integrated HD video and image recording .................................................................. 144

7.4 Configuring the software for specific users ...................................................................... 1467.4.1 Configuring the 14-function foot control panel ............................................................................. 1477.4.2 Configuring the handgrips............................................................................................................. 1477.4.3 Configuring image inversion on the Invertertube E ........................................................................ 1487.4.4 Configuring the direction of the XY coupling................................................................................. 1497.4.5 Configuring speeds........................................................................................................................ 1497.4.6 Configuring the speed of the RESIGHT 700 internal focus.............................................................. 1497.4.7 Configuring the overhead display .................................................................................................. 1507.4.8 Configuring fast focus ................................................................................................................... 1507.4.9 Configuring links ........................................................................................................................... 1517.4.10 Configuring reset options .............................................................................................................. 152

7.5 Daily operation ................................................................................................................. 1527.5.1 Setting the illumination ................................................................................................................. 1537.5.2 Setting the total magnification ...................................................................................................... 1577.5.3 Setting DeepView.......................................................................................................................... 1587.5.4 Setting the focus distance ............................................................................................................. 1597.5.5 Changing the XY coupling position ............................................................................................... 1597.5.6 Setting the integrated keratoscope ring......................................................................................... 1607.5.7 Setting the HD Digizoom............................................................................................................... 1617.5.8 Setting the integrated HD camera ................................................................................................. 1617.5.9 Recording...................................................................................................................................... 1657.5.10 Transferring control to CALLISTO eye ............................................................................................ 172


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7.5.11 Ending control via CALLISTO eye ................................................................................................... 173

7.6 Typical operating sequence .............................................................................................. 1747.6.1 Starting work ................................................................................................................................ 1747.6.2 Carrying out the working steps...................................................................................................... 1757.6.3 Stopping work .............................................................................................................................. 175

7.7 Switching the device off ................................................................................................... 176

8 Cleaning and disinfection ......................................................................... 177

8.1 Safety during cleaning and disinfection............................................................................ 177

8.2 Cleaning ........................................................................................................................... 1778.2.1 Cleaning optical surfaces ............................................................................................................... 1778.2.2 Cleaning mechanical surfaces ........................................................................................................ 1778.2.3 Fogging of optical surfaces............................................................................................................ 177

8.3 Disinfection ...................................................................................................................... 1788.3.1 Disinfection of surfaces ................................................................................................................. 178

9 Maintenance ............................................................................................ 179

9.1 Maintenance schedule for the operator............................................................................ 1799.1.1 Every six months............................................................................................................................ 179

9.2 Maintenance schedule for the authorized service............................................................. 1799.2.1 Every six months............................................................................................................................ 1799.2.2 Every twelve months ..................................................................................................................... 1799.2.3 Every two years ............................................................................................................................. 1819.2.4 Every four years............................................................................................................................. 1819.2.5 Every six years ............................................................................................................................... 181

9.3 Performing safety inspections .......................................................................................... 181

10 Troubleshooting....................................................................................... 183

10.1 Localizing malfunctions .................................................................................................... 18310.1.1 Response to faults with messages ................................................................................................. 18310.1.2 Exporting log files.......................................................................................................................... 183

10.2 Faults (with messages) ..................................................................................................... 184

10.3 Faults (without messages) ................................................................................................ 18510.3.1 Device faults.................................................................................................................................. 18510.3.2 Integrated HD video and image recording faults............................................................................ 18710.3.3 14-function foot control panel faults ............................................................................................. 18810.3.4 Wired 14-function foot control panel faults................................................................................... 189

10.4 Troubleshooting work ...................................................................................................... 19010.4.1 Activating manual mode................................................................................................................ 19010.4.2 Operating the device in manual mode ........................................................................................... 19110.4.3 Changing the halogen lamp .......................................................................................................... 19210.4.4 Swiveling the backup xenon lamp into position and resetting the remaining service hours ............ 19310.4.5 Changing the Superlux Eye light source lamp module.................................................................... 19410.4.6 Setting the gas spring on the integrated 22" monitor .................................................................... 19510.4.7 Increasing mobility of the suspension arm on the integrated 22" monitor .................................... 19610.4.8 Increasing mobility of the monitor mount on the integrated 22" monitor ...................................... 197


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10.4.9 Increasing mobility of the monitor mount on the integrated CALLISTO eye Panel PC support arm . 19710.4.10 Establishing cable connections for the 14-function foot control panel ........................................... 19810.4.11 Displaying the firmware versions ................................................................................................... 19810.4.12 Opening the service menu............................................................................................................. 198

11 Technical specifications............................................................................ 201

11.1 Essential performance features ........................................................................................ 201

11.2 Compliance....................................................................................................................... 201

11.3 Electrical data................................................................................................................... 20211.3.1 Stand ............................................................................................................................................ 20211.3.2 Light sources ................................................................................................................................. 20211.3.3 Integrated HD camera ................................................................................................................... 20311.3.4 Integrated HD video and image recording ..................................................................................... 20411.3.5 Integrated keratoscope ring .......................................................................................................... 20511.3.6 Integrated 22" monitor ................................................................................................................. 205

11.4 Mechanical data ............................................................................................................... 20511.4.1 Integrated slit illumination ............................................................................................................. 20511.4.2 Integrated 22" monitor ................................................................................................................. 205

11.5 Optical data...................................................................................................................... 20611.5.1 Surgical microscope....................................................................................................................... 20611.5.2 Objective lenses............................................................................................................................. 20611.5.3 Objective lenses with support ring................................................................................................. 20611.5.4 Eyepieces ...................................................................................................................................... 206

11.6 Dimensions and weights................................................................................................... 20711.6.1 Dimensions and swiveling ranges .................................................................................................. 20711.6.2 Support arm for integrated CALLISTO eye Panel PC ....................................................................... 20811.6.3 Support arm for integrated 22" monitor........................................................................................ 20911.6.4 Maximum weight capacity............................................................................................................. 21011.6.5 Total weight.................................................................................................................................. 210

11.7 Ambient requirements for operation ................................................................................ 211

11.8 Ambient requirements for transport and storage ............................................................. 211

11.9 Guidance and manufacturer´s declaration – electromagnetic immunity............................ 21111.9.1 EMC - electromagnetic compatibility IEC 60601-1-2 ...................................................................... 213

12 Accessories and spare parts ..................................................................... 215

12.1 Accessories ....................................................................................................................... 21512.1.1 Video accessories .......................................................................................................................... 21512.1.2 14-function foot control panel ...................................................................................................... 21512.1.3 Fundus viewing systems ................................................................................................................ 21512.1.4 Additional illumination .................................................................................................................. 21512.1.5 Sterilizable caps............................................................................................................................. 21612.1.6 Drapes........................................................................................................................................... 216

12.2 Spare parts ....................................................................................................................... 21612.2.1 Lamps and light guides.................................................................................................................. 21612.2.2 Dust cover..................................................................................................................................... 21612.2.3 Network cable............................................................................................................................... 21612.2.4 Country-specific power cable......................................................................................................... 217


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12.3 Components ..................................................................................................................... 21712.3.1 Tubes for surgical and assistant's microscopes............................................................................... 21712.3.2 Eyepieces for surgical and assistant's microscopes ......................................................................... 21712.3.3 Intermediate pieces for surgical microscope .................................................................................. 21712.3.4 Objective lenses............................................................................................................................. 21812.3.5 Coobservation ............................................................................................................................... 21812.3.6 Integrated components (factory installed)...................................................................................... 21812.3.7 CALLISTO eye ................................................................................................................................ 219

12.4 UC kits .............................................................................................................................. 219

13 Decommissioning ..................................................................................... 221

13.1 Cleaning before storage ................................................................................................... 22113.1.1 Cleaning the device and accessories .............................................................................................. 221

14 Packaging and transport.......................................................................... 223

14.1 Preparing for transport..................................................................................................... 22314.1.1 Placing the device in the transport position ................................................................................... 223

15 Disposal ................................................................................................... 225

15.1 Disposal of the device....................................................................................................... 225

Glossary ................................................................................................... 227

Keyword index ......................................................................................... 231

Empty page, for your notes

Instructions for Use 1 Notes on Instructions for UseOPMI LUMERA 700 1.1 Device name

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1 Notes on Instructions for Use

1.1 Device nameOPMI LUMERA 700 is referred to as "device" in the present Instruc-tions for Use

1.2 Area of applicationThe present Instructions for Use apply to OPMI LUMERA 700 withSoftware Release 3.1 and the following identification:

• Reference number: 6634 OPMI LUMERA 700

1.3 Purpose and storage of the documentationThese Instructions for Use explain the safety features, functions andperformance parameters of the device. They contain instructions onthe safe use of the device and identify measures for its care andmaintenance.

Correct operation of the device is imperative for its safe andsuccessful function.

u Read these Instructions for Use before setting up and using thedevice the first time.

u Keep the Instructions for Use accessible for all users at all times.

u Pass the Instructions for Use to future owners of the device.

1.4 Questions and commentsu If you have any questions or comments concerning these

Instructions for Use or the device itself, please contact ZEISSService.

You can find the ZEISS contact partner for your country on thefollowing website: www.zeiss.com/med

1.5 Conventions in this documentCertain types of information are specially marked in this documentfor better recognition.

1.5.1 Conventions in all text areas• This is a list.

– This is a second level list.

This is a cross-reference: Questions and comments [} 11].

This is bold type.

This is software code or program text.

1 Notes on Instructions for Use Instructions for UseOPMI LUMERA 7001.5 Conventions in this document

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Names of software dialogs, fields or menus, and softwaremessages are marked by quotation marks:

• "View" menu.

• "Do you want to save the settings?"

The steps in menu and file paths are separated by slashes:

• "File / Save as"

• "My documents / Documents"

Keys, buttons, knobs, levers and other operating controls aremarked by square brackets:

• [START] key

• [Next] button

1.5.2 Conventions in a course of action

WARNING! This is warning information about hazards that can causedeath or severe injuries if not avoided.

The warning message names the possible consequences.

u This is a measure with which hazards can be prevented.

CAUTION! This is warning information about hazards that can causeinjuries if not avoided.



NOTE This is warning information about hazards that can causeproperty damages if not avoided.



þ This is a requirement that must be met before the start of asequence of actions.

1. This is a command.

2. CAUTION! This is a warning message about hazards thatcan occur during a single action. This is a command.

ð This is the result of a sequence of actions.

Instructions for Use 1 Notes on Instructions for UseOPMI LUMERA 700 1.6 Other applicable documents

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1.6 Other applicable documentsDocument type Document title Optional

Product overview ZEISS Video Accessories No

Instructions for Use Preparation of Resteril-izable Products

No

Instructions for Use VISULUX Yes

Instructions for Use RESIGHT 500 &RESIGHT 700

Yes

Instructions for Use CALLISTO eye Yes

Instructions for Use CALLISTO eye Panel PC(model I)

Yes

Instructions for Use CALLISTO eye Panel PC(model II)

Yes

Instructions for Use CALLISTO eye BasicFunctions

Yes

Instructions for Use CALLISTO eye - SoftwareAdd-On for AssistanceFunctions

Yes

Instructions for Use CALLISTO eye - SoftwareAdd-On forOPMI LUMERA 700 Control

Yes

Instructions for Use CALLISTO eye - SoftwareAdd-On for VISALIS 500Parameter Display

Yes

Instructions for Use 2 Safety notesOPMI LUMERA 700 2.1 Target group

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2 Safety notes

2.1 Target groupThese Instructions for Use are intended for physicians, medical andtechnical staff, and nurses who are responsible for preparing,operating or maintaining the device following training.

It is the duty of the equipment owner/operator to train and instructall operating personnel.

2.2 Area of use

2.2.1 Intended useThe OPMI LUMERA 700 is a surgical microscope designed for theillumination and magnification of the surgical area and for thesupport of visualization in surgical procedures in the field ofophthalmology.

2.2.2 Normal useOn account of its mechanical construction and the characteristicslisted below, the device is suited for performing surgical procedureson the anterior and posterior segments of the eye:

• SCI illumination system (Stereo Coaxial Illumination)

• A range of illumination sources

• Attachable fundus viewing systems (RESIGHT 500,RESIGHT 700)

Once the power switch has been activated, the device can be safelyand easily moved into its operating position after the magneticbrakes have been released, either by using the handgrips or thesuspension arm. Before the start of surgery, a sterile personnelmember covers the microscope with drapes and applies resteril-izable caps.

The surgeon or a sterile personnel member positions themicroscope and focuses it. During surgery, the most frequentlyused operator functions, such as focus, magnification, XYmovement, light intensity up/down and adjustment of the illumi-nation level, are controlled by means of the foot control panel,allowing the hands to remain free for operating. Certain settings,such as the illumination level, unlocking of the magnetic brakes orthe insertion of RESIGHT 500 or RESIGHT 700 for surgical proce-dures conducted on the anterior segment of the eye, are made byhand. Additional video accessories can be attached to the devicefor training purposes or to visually display the progress of surgeryfor personnel.

2 Safety notes Instructions for UseOPMI LUMERA 7002.3 Responsibilities and duties of the operator

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When finished, the surgeon swivels the microscope out of thesurgical field and into the park position. Pressing the reset buttonon the XY coupling, or positioning the device in the park position,resets the device to its initial values and makes it ready for the nextoperation. The drape or the resterilizable caps are removed by thesurgeon or by a nurse. The drape is to be disposed of in accordancewith the hospital regulations of the respective country. The resteril-izable caps can be sterilized again. The device can be cleaned anddisinfected.

The product must be regularly checked for full functionality by ahospital technician.

At the end of the electronic device's service life, it must be disposedof in accordance with the regulations of the respective country.

2.3 Responsibilities and duties of the operator

Operating personnel

The device may be operated only by properly instructed and trainedpersons.

u Make sure that the operating personnel are appropriatelytrained and instructed.

u Make sure that the operating personnel have read and under-stood the Instructions for Use.

u Keep the Instructions for Use available at all times for theoperating personnel.

u To facilitate access for all operating personnel: Requestadditional copies of the Instructions for Use as required fromZEISS.

u Specify the competencies for handling the device and statewho is authorized to perform what tasks.

u Determine the reporting obligations for malfunction anddamage and make them known. Notification of the manufac-turer and authorities. [} 17]

u Provide the necessary protective clothing.

u Regularly check that the legal regulations applicable in yourcountry with regard to accident prevention and work safety arebeing complied with.

Safety inspections

u To prevent a decrease in device safety due to aging and wear:Implement regular safety inspections as specified for this deviceby the applicable national regulations.

The safety inspections may only be performed by the manufactureror qualified personnel.

u Comply with the specified time limits.

Instructions for Use 2 Safety notesOPMI LUMERA 700 2.3 Responsibilities and duties of the operator

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u Carry out checks according to the extent specified.

The safety inspections of the device should at least comprise thefollowing points:

• Availability of the Instructions for Use

• Visual inspection of the device and accessories for damage, aswell as legibility of the labels

• Leakage current test

• Test of protective ground conductor

• Function and wear test of the brakes

• Function test of all switches, buttons, sockets and indicatorlamps of the device

Maintenance and inspection

u To ensure safe operation of the device and reach the expectedservice life: Comply with the maintenance and inspectionintervals specified in these Instructions for Use.

Modifications to the product

u WARNING: This device must not be modified without themanufacturer’s approval. If the device is modified, suitableinspections and testing must be completed to ensure that it canstill be used safely.

Accessories and additional equipment

u If you want to connect accessories or additional equipment tothe device: Contact your ZEISS contact partner [} 11].

Any additional equipment connected to medical electrical devicesmust demonstrably comply with the applicable IEC or ISO standards(e.g. IEC 60950 for data processing equipment).

In addition, all configurations must meet the normative require-ments for medical systems (see IEC 60601-1-1 or Clause 16 of the3rd edition of IEC 60601-1 respectively).

Anyone connecting additional equipment to medical electricalsystems is a system configurer and as such responsible forcompliance of the system with the standards for systems.

Local legislation has priority over the above normative require-ments.

2.3.1 Messages to manufacturer and authoritiesIf a serious incident occurs in connection with this medical deviceaffecting the operator or another person, the operator (or personresponsible) must report this serious incidence to the manufactureror seller of the medical product. In the European Union, theoperator must report this serious incident to the responsibleauthorities in the applicable country.

2 Safety notes Instructions for UseOPMI LUMERA 7002.4 Measures and duties of the operator

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2.4 Measures and duties of the operator

Electrical safety

u Always switch off the device before connecting it to or discon-necting it from the power supply, for cleaning its surface, or ifit will not be used for a prolonged period of time.

u Only connect the device to a power supply that complies withthe values specified on the rating label.

u Do not use multiple sockets!

u Do not use extension cables!

u Do not touch the device if your body is electrostatically chargedand the device is not grounded.

u Connect the device via the potential equalization connection(according to IEC 60601-1) to other active devices with thesame ground potential or connect it to a protective groundconnection.

u Please observe the information on electromagnetic compati-bility (EMC).

The device contains freely accessible live components. If youremove the housing, you run the risk of electric shock.

u Never open the device!

Environmental conditions

u Make sure that the installation conditions and the operation ofthe device comply with the surgical requirements:

• Low vibration

• Clean environment

• Avoid extreme mechanical stress

u Do not use power-operated devices included in the deliverypackage

• in explosive atmospheres,

• at a distance of less than 25 cm from flammable anesthetics orvolatile solvents such as alcohol, benzine or similar substances.

u Do not use or store the device in damp rooms. Do not exposethe device to water splashes, dripping water or sprayed water.

u Ensure that fluids cannot enter the device.

Symbols and labels

u Note the symbols and labels attached to the device!

Instructions for Use 2 Safety notesOPMI LUMERA 700 2.5 Electromagnetic compatibility

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Transport

u Only transport the device over long distances (e.g. relocation,return for repair) in its original packaging or special returnpackaging.

u Please contact your dealer or ZEISS Service for this purpose.

2.5 Electromagnetic compatibilityThe device is subject to special requirements regarding electromag-netic compatibility (EMC). The following factors can cause EMCdisturbances:

• Portable and mobile HF communication equipment in thevicinity of the device.

• Other devices set up in the vicinity or stacked together with thedevice.

• Accessories, cables and spare parts not specified in the Instruc-tions for Use and not sold by ZEISS as spare parts.

You can prevent EMC disturbances by using the following precau-tionary measures:

u Please comply with the Instructions for Use.

u Observe the EMC guidelines in the Technical Specificationschapter.

u Only use accessories, transformers, cables and spare partsspecified in the Instructions for Use or approved by ZEISS forthis device.

u If you are using radio communication equipment or compo-nents for radio transmission: Keep a distance of 30 cm to allcomponents of the device.

u If you are installing the device near or stacking it with otherdevices: Check to make sure the device is operating correctly inthis configuration.

2.6 Requirements for operation

2.6.1 Before commissioning for the first time

Installation performed by technical personnel or ZEISSService

Please make sure that the following requirements continue to bemet for further operation:

u Make sure that the connecting components are properly setand that all screw connections are securely tightened.

u Make sure that all cables and plugs are in proper condition.

2 Safety notes Instructions for UseOPMI LUMERA 7002.6 Requirements for operation

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u Make sure that the device is connected to an electrical outletwith a proper protective ground conductor.

u Determine the supply voltage at the installation site and set thevoltage of the device in accordance with the installation site'ssupply voltage.

u Make sure the device is connected using the provided powercable.

Hazards arising from connecting the device to an IT network

The following safety measures should be observed in order toprevent injuries or damage:

u Check to make sure that the requirements for connecting thedevice to an IT network are met. [} 90]

Hazards arising from condensation of air humidity

Moving the device from a cold environment (T < 10 °C) to a warmone may cause air humidity to condense.

u If you move the device from a cold environment to a warmone, wait at least one hour before switching the device on toallow it to reach the environment's ambient temperature.

2.6.2 Before every use

Hazards arising from phototoxicity

To prevent phototoxic damage to the patient's eye:

u Check the light source for visible damage.

u Check the filter setting.

u Switch off the light source for light guides that are not beingused and attach them to the mount provided.

Hazards arising from attached accessories and components


u Never exceed the device's maximum permitted weight load.

u Always route cables so that they do not hinder the user.

u Never cover any ventilation openings. Doing so can cause thedevice to overheat and fail.

u Never attempt to forcefully connect any electrical connectors. Ifa connection cannot be made, check to make sure the plug fitsthe socket. If any of the connectors are damaged, have theZEISS Service team or an authorized service representativerepair them.

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Hazards arising from moving components


u Make certain to compensate for any added weight to thedevice; this will enable the surgical microscope to maintain itsbalance in all positions of the working range.

u Limit the stroke of the suspension arm to prevent any contactwith the patient should the surgical microscope be loweredaccidentally.

u Check the surgical microscope for sufficient freedom ofmovement.

u Make sure there is sufficient space available for focuspositioning. The surgical microscope must not come intocontact with the patient.

u Secure the device into position using the locking tabs on thestand base to prevent the device from rolling awayunexpectedly.

u When using a fundus viewing system: make sure that the spaceavailable for movement is greater than the downward travelpath of the microscope.

u When using an assistant's microscope: adjust the assistant’smicroscope before use and make sure it is properly locked inposition. If you tilt the surgical microscope in the horizontalviewing direction and the assistant’s microscope is not lockedin place, the assistant's microscope may swivel in.

Hazards arising from an attached fundus viewing system

Incorrect handling of a fundus viewing system mounted on theunderside of the microscope, or activation of the fast focus, maycause injury to the patient’s eye.

u Before using a fundus viewing system, make sure that thespace available for movement is greater than the downwardtravel path of the microscope.

u Perform a focus reset.

Hazards arising from disruptions to the 14-function footcontrol panel

Inadequate power supply to the 14-function foot control panel maycause the device to malfunction.

u Make sure that the batteries are fully charged and that the"Battery" status display is not blinking.

Hazards arising from unknown software settings


2 Safety notes Instructions for UseOPMI LUMERA 7002.6 Requirements for operation

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u Before each use, check the user settings in the software.

Dangers arising from unchecked functions

To avoid injury or damage, please observe the following safetymeasures.

u Perform a function test of the device prior to use.

2.6.3 During operation

Hazards arising from phototoxicity

To prevent phototoxic damage to the patient's eye:

u Use the lowest brightness setting possible.

u Select an appropriate brightness setting according to therecommended values provided by ZEISS (see "Maximumradiation exposure times" [} 27]). Doing this limits theexposure intensity and the exposure time.

u Use the retina protection filter to reduce the blue portions ofthe light. The retina protection filter protects the patient’s eyefrom unnecessary radiation and increases the exposure time.

u When working on the exterior eye: use the retina protectiondevice. This will prevent light from entering the pupil.

u Avoid looking directly into the light source on the microscope'sobjective lens or light guide.

u When the light source is switched on: monitor the device at alltimes.

Hazards arising from unsterile parts

Unsterile parts may cause injury to the patient.

u Always use the appropriate sterile accessories for the device.

u Never touch the unsterile connection cable on the assistant'smicroscope while operating the handgrips or zoom button.

Hazards arising from the fundus viewing system swiveling in

If the RESIGHT 500 or RESIGHT 700 fundus viewing system ismounted on the underside of the microscope, and you steeply tiltthe microscope, the RESIGHT fundus viewing system may uninten-tionally swivel in and injure the patient.

u Remove the fundus viewing system before tilting themicroscope at a steep angle.

Hazards arising from defective or unidentified accessories

Defective or unidentified accessories may lead to increased leakagecurrent on the device and injure the patient.

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u Do not connect any defective or unidentified accessories.

u Never touch the video interfaces while you are in contact withthe patient.

u Never touch the power outlet while you are in contact with thepatient.

Hazards arising from defective motor electronics

Defective motor electronics can cause limited functionality andfailure of the following primary functions:

• XY movement

• Focus

• Zoom

• Light control

u Activate manual mode.

Hazards arising from an outdated xenon lamp

If the xenon lamp is used beyond its maximum service life of 500hours, it may fail suddenly and interrupt operation.

u When the xenon lamp has reached 5 operating hours: swivelthe backup xenon lamp into position.

u When the backup xenon lamp has reached 5 operating hours:replace the xenon lamp module of the Superlux Eye lightsource and reset the remaining service hours meter to its initialvalue.

Hazards caused by a hot halogen lamp

If you replace the lamp shortly after it has failed, the lamp will stillbe very hot.

u Use heat-resistant protective gloves when replacing the lamp.

Hazards caused by a not fully functional device

If an error occurs which cannot be fixed by using the"Troubleshooting" section:

u Mark the device as non-functional.

u Notify ZEISS Service or an authorized service representative.

2.6.4 After every use

Hazards arising from a lack of supervision

If the device is switched on, but not supervised, it may causeinjuries or damage.

2 Safety notes Instructions for UseOPMI LUMERA 7002.7 Measures to prevent phototoxic injury

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u If you are not using the device, switch it off at the powerswitch.

Hazards arising from inadequate sanitation

Insufficient, incorrect or wrong cleaning or disinfection that doesnot comply with these Instructions for Use can expose the patientor medical staff to a considerable risk of infection.

u Follow the instructions in "Cleaning and disinfection [} 177]".

2.7 Measures to prevent phototoxic injuryThere are multiple publications [} 28]1-5) that deal with the issue ofphototoxicity in eye surgeries. They list five aspects of particularconcern:

• Illumination characteristics (spectral composition)

• Illumination intensity

• Angle of illumination

• Focus of the light source

• Exposure time to light

In the following, comments on these aspects are given and adescription of how ZEISS, as a manufacturer, makes allowance forthem in its systems.

2.7.1 Illumination characteristics (spectral composition)Studies on exposing the eye to light with varying spectral composi-tions have been conducted since as early as the 1950s. Thesestudies suggest that the potential hazard of phototoxic injury to thepatient's retina can be reduced by blocking out the blue and ultra-violet light below a wavelength of 475 nm.

Integrated protection filters

For protection of the retina, ZEISS offers the swing-in retinaprotection filter (blue barrier filter) and the stationary UV blockingfilter as standard features of the surgical microscope. This reducesnot only the exposure of the patient's eye to light, but also that ofthe surgeon.

The retina protection filter's orange color changes the color of thelight. The physician must become accustomed to working with thealtered appearance of the anatomical structures.

2.7.2 Illumination intensityThe majority of researchers suggest that the surgeon should usethe lowest light intensity required on the patient's eye to guaranteeoptimal viewing during surgery.

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Brightness control

ZEISS has addressed this aspect by providing its devices with afeature for continuously varying the brightness of the light source.This permits the surgeon to optimally adapt the light intensity onthe patient's eye to the conditions existing in each case.

2.7.3 Angle of illuminationA number of publications [} 28] 1-4) suggest tilting the microscopeto reduce the exposure of the macula to direct illumination.

Tilting mechanism

The surgical microscope features a tilting mechanism for the mainmicroscope to enable indirect illumination.

2.7.4 Focus of the light sourceStudies show that injuries are likely to occur if the filament of thelight source is imaged on the patient's retina. The peak intensity ofa filament is considerably higher than that of an even and extendedlight source.

Fiber optic illumination

For this reason, ZEISS uses fiber optic illumination in its surgicalmicroscope systems.

2.7.5 Exposure time to lightAccording to some publications, the eye should not be exposed tothe light source longer than a few minutes. In all surgical cases, theretinal exposure time to light depends on the type and duration ofthe procedure and possible case complications.

It is therefore recommended in ophthalmic surgery to keep thelight intensity as low as possible, or to use a device which preventsthe light from entering the patient's pupil. It is also recommendedto make sure that the patient's eye is not additionally exposed tothe light of surrounding light sources.

This problem has been solved by ZEISS through the use of a swing-in retina protection filter (blue barrier filter) that can be swung intothe microscope's illumination beam path.

Brightness setting

The brightness control scale of our devices has a linear structurewith values ranging from 2% to 100% for LED light sources and5% to 100% for xenon/halogen light sources. The stipulations ofstandard DIN EN ISO 15004-2:2007 result in maximum radiationexposure times for the different illumination configurations. Thesecan be found in the table "Maximum radiation exposure times[} 27]".

2 Safety notes Instructions for UseOPMI LUMERA 7002.7 Measures to prevent phototoxic injury

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Phototoxic risk factors

The microscope light source—like any bright light source—maypresent a potential hazard to the patient’s eye both in the form ofimmediately visible thermal damage to the retina as well as photo-toxic chemical reactions which may lead to photoretinitis. Thefactors which play an important role in determining the phototoxicrisk are:

• Lamp brightness

• Spectral distribution of the light (UV and blue light are moredangerous than longer wavelengths)

• Duration of direct exposure

• Pupil size

• Clarity of ocular media (infants and young children, forexample, may be at a higher risk)

• Condition of the eye (aphakic and pseudo-aphakic eyes withIOLs of a material without UV / blue filter are at a higher risk)

• Previous exposure to bright light (such as retinal photography,especially within the last 24 hours)

During cataract procedures, exposure is interrupted by thefollowing factors:

• Lens material

• Phaco handpiece

• Eye movement

This is expected to significantly lengthen the time before photore-tinitis might be expected to occur.

Effects of microscope illumination

A prospective study [} 29] 7) of the effects of microscope illumi-nation during surgery did not reveal any phototoxic retinal injuriesfor procedure times of up to 30 minutes if the calculated maximumrecommended exposure time was 150 seconds. The prospectivestudy also found that, at the same brightness setting, phototoxicretinal injury could be expected after operations with a duration ofapproximately 100 min.

Stereo Coaxial Illumination (SCI)

The Stereo Coaxial Illumination of this device has been designed toprovide a bright red reflex using only very small quantities of lightin the center of the surgical field.

The peripheral illumination causes higher exposure of the retina,but, depending on the position of the eye, usually not the maculadirectly. In order to reduce the risk of phototoxicity during cataractoperations, ZEISS recommends taking the following measures:

Instructions for Use 2 Safety notesOPMI LUMERA 700 2.8 Maximum radiation exposure

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u Adjust the surrounding field illumination to be somewhatdarker than the central red reflex spot. This simultaneouslyreduces glare from the patient's sclera.


u Use the retina protection filter (blue barrier filter) to reduce theblue portions of the light. The retina protection filter increasesthe recommended duration of the radiation exposure.


u Turn off the microscope illumination system or cover thepatient’s eye during pauses in surgery.

2.8 Maximum radiation exposureThe following tables are intended to serve as guidelines for deter-mining potential hazards.

Bases for calculation

The calculations are based on the daily exposure [} 29] limitsrecommended for occupational safety6). A safety factor of 10 hasbeen used in determining these limits.

The data has been calculated for the worst case scenario:

• Direct exposure

• Uninterrupted exposure (no surgical instruments in the eye)

• Aphakic eye

• Immobile eye (exposure in one area only)

• Pupil dilated to 8 mm

2.8.1 Maximum radiation exposure times with red reflexillumination

Brightnesslevel [%]

Maximum exposure times per light source [min]

Halogen Xenon LED XenonwithHaModefilter

LED withHaModefilter

25 47.0 7.6 19.7 26.6 69.7

50 21.3 3.7 9.9 12.9 34.8

75 12.9 2.8 6.6 9.8 23.2

100 9.2 2.0 5.0 2.0 17.4

The use of the retina protection filter increases the recommendedexposure time by a factor of 5. Any deviation from these values isonly permissible when medically justified.

2 Safety notes Instructions for UseOPMI LUMERA 7002.8 Maximum radiation exposure

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2.8.2 Maximum radiation exposure times with surroundingfield illumination

Brightnesslevel [%]




25 13.7 2.3 6.0 8.0 20.7

50 6.2 1.1 3.0 3.8 10.3

75 3.8 0.8 2.0 2.8 6.9

100 2.7 0.6 1.5 2.1 5.1


2.8.3 Maximum radiation exposure times with integrated slitilluminator

Brightnesslevel [%]




25 18.4 3.3 8.6 11.5 31.0

50 8.2 1.6 4.3 5.6 15.5

75 5.1 1.2 2.9 4.2 10.3

100 3.6 0.9 2.1 3.1 7.7


2.8.4 References1) H. Stiller and B. Rassow

• "Light hazards to the patient's retina from ophthalmic instru-ments," Applied Optics-OT 30, 2187-2196 (1991)

2) American Conference of Governmental Industrial Hygienists

• "Documentation of the Threshold Limit Values for PhysicalAgents. 7th Edition," (American Conference of GovernmentalIndustrial Hygienists, Cincinnati, 2001)

3) S. G. Khwarg, F. A. Linstone, S. A. Daniels, S. J. Isenberg, T. A.Hanscom, M. Geoghegan, and B. R. Straatsma

Instructions for Use 2 Safety notesOPMI LUMERA 700 2.8 Maximum radiation exposure

G-30-1673-en - 14.0 - 2018-07-12 29 / 236

• "Incidence, risk factors, and morphology in operatingmicroscope light retinopathy," Am. J. Ophthalmol. 103,255-263 (1987)

4) G. Kleinmann, P. Hoffman, E. Schechtman, and A. Pollack

• "Microscope induced retinal phototoxicity in cataract surgery ofshort duration," Ophthalmology 109, 334-338 (2002)

5) DIN EN ISO 15004-2:2007 Optical instruments -- Fundamentalrequirements and test methods

• Part 2: Light hazard protection6) David Sliney, Danielle Aron-Rosa, Francois DeLori, FranzFankhauser, Robert Landry, Martin Mainster, John Marshall,Bernard Rassow, Bruce Stuck, Stephen Trokel, Teresa Motz West,and Michael Wolffe

• Adjustment of guidelines for exposure of the eye to opticalradiation from ocular instruments: statement from a task groupof the International Commission on Non-Ionizing RadiationProtection (ICNIRP) APPLIED OPTICS Vol. 44, No. 11, p 2162 (10April 2005)

7) Byrnes, G.A., Antoszyk, A.N., Mazur, D.O., Kao, T.C., Miller, S.A.

• Photic maculopathy after extracapsular cataract surgery. Aprospective study, 1992/ 05/01 Ophthalmology, VL - 99, IS - 5,SP - 731, EP - 737, PB - Elsevier

Instructions for Use 3 Description of the deviceOPMI LUMERA 700 3.1 Device marking

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3 Description of the device

3.1 Device marking

CAUTION! Risk of injury due to illegible labels!

Over time, labels can become dirty or unidentifiable, making itdifficult or impossible for hazards to be recognized or necessaryoperating instructions to be followed.

u For this reason, all safety, warning and operating instructionsare to be kept in good condition at all times.

u Damaged labels are to be replaced immediately. Forreplacement labels, contact us or one of our authorized repre-sentatives.

Symbol Name Explanation

Warninglabel

General warning symbol!

Warninglabel

Warning against hand injuries!

Warninglabel

Hot surface warning!

Warninglabel

Maximum load capacity 13 kg!

Warninglabel

Maximum load capacity 9 kg!

Mandatorysign

Consult Instructions for Use

Symbol Observe the Instructions for Use oraccompanying documents.

• Manual mode fault signal [} 52]

• LED light source fault signal [} 51]

• [Downward travel limit] rotary knob[} 60]

• [Open lamp module] button [} 64]

• Invertertube E port [} 47]

3 Description of the device Instructions for UseOPMI LUMERA 7003.1 Device marking

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Rating label Provides information on:

• Manufacturer

• Device data

• Performance data [} 202]

• Device conformity [} 201]

UDI label Provides information on:

• Date of manufacture

• Machine readable label (barcode)

• UDI Device Identifier (UDI-DI)

• UDI Production Identifier (UDI-PI)

SIP label Provides information on:

• Manufacturer

• Manufacturer’s contact details

• SIP number of the device

Lampchange

u Press the button

u Pull out the lamp module

u Rotate [Backup Xenon Lamp] switch180°

Transportposition

Set the device to this position prior totransport in order to prevent damage.

1-Chip HDCamera

The device includes an integrated 1-chipHD camera.

HD camera The device includes an integrated 3-chipHD camera.

HDrecording

The device includes integrated HD videoand image recording.

IDIS The device includes IDIS.

Manufac-turer

-

Instructions for Use 3 Description of the deviceOPMI LUMERA 700 3.1 Device marking

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WEEE label Do not dispose of electrical and electronicdevices with normal domestic waste. Thebar beneath the garbage bin icon declaresthat the device was "put into circulation"on August 13, 2005.

Non-ionizingelectromag-neticradiation

-

Serialnumber

-

Referencenumber

-

CE marking -

CSA certifi-cation mark

-

Pairing Pairs the device with the FCP WL footcontrol panel.

Focusposition

If the dot is located between the twoarrow tips, the surgical microscope'sfocusing system is in its initial position.

Front-to-back tilt axis

If the line matches the line on the supportarm, the surgical microscope is in thevertical position.

Unlocked -

Locked -

Lamp -

Serviceinterface

-

3 Description of the device Instructions for UseOPMI LUMERA 7003.1 Device marking

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Foot controlpanelconnector

-

Signaloutput andinput

-

Signaloutput

-

Signal input -

Potentialequalization

-

USB USB port -

LAN 1 Networkconnection

-

LAN 2 Networkconnection

-

HD-SDI Signaloutput

-

100V -240Vmax.

500VA

Poweroutput

For connecting devices with the correctelectrical ratings.

- Radio label See also document G-30-2021 (RadioApproval Information)

Instructions for Use 3 Description of the deviceOPMI LUMERA 700 3.2 Device setup

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3.2 Device setup

2 3

10

11

12

13

1 4

5

6

7

8

9

Figure 1: Example with integrated CALLISTO eye Panel PC and assistant's microscope

1 CALLISTO eye Panel PC (model II) 2 Support arm for CALLISTO eye Panel PC

3 Lamp housing 4 Suspension arm

5 XY coupling 6 Overhead display

7 Surgical microscope 8 Assistant's microscope

9 14-function foot control panel 10 Stand base

11 Stand column 12 Support arm with connector panel

13 Control panel

The following components can alternatively be attached for theCALLISTO eye Panel PC (model II):

• CALLISTO eye Panel PC (model I)

• 22" monitor

• 22" monitor with instrument tray

3 Description of the device Instructions for UseOPMI LUMERA 7003.2 Device setup

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3.2.1 CALLISTO eye Panel PCThe CALLISTO eye Panel PC provides hardware and interfaces forthe device. This hardware enables the device to receive, record andplay back video signals generated during surgery.

2

1

2

1

Figure 2: CALLISTO eye Panel PC (pictured left: model I, pictured right:model II)

1 User terminal 2 Touch screen

3.2.2 Support arm for CALLISTO eye Panel PCThe support arm is used to orient the CALLISTO eye panel PC verti-cally or horizontally.

1 2

34

Figure 3: Support arm for CALLISTO eye Panel PC

1 VESA interface 2 Monitor mount

3 Suspension arm 4 Fixing lever


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3.2.3 Lamp housingThe lamp housing is used to store the light sources. Simple lightsources supply light to the surgical microscope's SCI illuminationsystem. Dual light sources supply light to the surgical microscope'sSCI illumination system as well as an additional illumination system.

1 2 3

Figure 4: Simple light sources

4 5 6

7

Figure 5: Dual light sources

1 Superlux Eye 2 Halogen (optional)

3 LED (optional) 4 Superlux Eye + LED (optional)

5 Superlux Eye + Halogen(optional)

6 LED + LED (optional)

7 Halogen + LED (optional)


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3.2.3.1 Light source features

Feature Explanation Light source

SuperluxEye

Halogen LED

Lampchange

Manual Automatic

Automatic

3.2.3.2 Swivel filters

Filter Explanation Light source

SuperluxEye

Halogen LED

Retinaprotectionfilter

Protects the patient'seye from unnecessaryradiation and allowsthe recommendedexposure time to beincreased.

Standard Standard Standard

Fluores-cence filter485 nm

Makes fluorescentareas visible.

Optional Optional Optional

HaModefilter

Generates a lightspectrum similar to thatof a halogen lightsource.

If the filter is built in,the front panel containsthe label number304977-9116-500.

Standard - Standard

Gray filter25%

Reduces the set lightintensity to 25% andallows the radiationexposure time to beincreased by a factor of4.

- - Optional


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3.2.4 Suspension armThe suspension arm is used to position the microscope verticallyand horizontally.

1

2

3

Figure 6: Suspension arm

1 Magnetic brake 2 Cable tray

3 XY coupling interface

3.2.5 XY couplingThe XY coupling is used to orient the surgical microscope verticallyabove the patient's eye in the X and Y-direction.

1

2

Figure 7: XY coupling

1 Support arm for the surgicalmicroscope

2 Motorized positioning unit


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3.2.6 Overhead displayThe overhead display displays information on the device's softwaresettings.

1

Figure 8: Overhead display

1 Display

3.2.7 Surgical microscopeThe surgical microscope enlarges and illuminates the surgical field.

2

2

34

1

Figure 9: Surgical microscope (example with Invertertube E)

1 Invertertube E 2 Eyepieces

3 Main observer 4 Objective lens


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3.2.7.1 Invertertube E

The Invertertube E rotates inverted images into an upright position.

23

1

2

Figure 10: Invertertube E

1 Tube body 2 Eyepiece mount

3 Panning mechanism

The Invertertube E can be electrically swiveled 110°.

3.2.7.2 Widefield eyepiece (10x or 12.5x)

2

3

1

Figure 11: Widefield eyepiece (10x or 12.5x)

1 Magnetic coupling 2 Diopter scale

3 Eyecup


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3.2.7.3 Objective lens

The apochromatic lens adjusts the surgical microscope to fitdifferent operating distances.

1 2

Figure 12: Objective lens

1 Lens 2 Fine screw threads

3.2.8 Assistant's microscopeThe assistant's microscope provides the assistant with the sameimage as that of the main operator.

23

1

Figure 13: Assistant's microscope (example with Invertertube E)

1 Invertertube E 2 Swivel mechanism with lock

3 Electrical zoom system: works independently of, or in parallel with,the surgical microscope zoom feature. Alternative: manual 5x magnification changer: works indepen-dently of the surgical microscope's zoom feature.


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3.2.9 14-function foot control panelThe 14-function foot control panel is used to operate the devicehands free.

1

2

Figure 14: 14-function foot control panel

1 Bracket 2 Storage bracket

The 14-function foot control panel is available in wireless (FCP WL)and wired versions (FCP).

3.2.10 Stand base

1

23

Figure 15: Stand base

1 Locking tab 2 Cable deflector

3 Steerable casters


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3.2.11 Stand column

1

2

3

Figure 16: Stand column

1 Cable holder 2 Bracket for foot control panel

3 Transport handle

3.2.12 Support arm with connector panelThe support arm is used to orient the suspension arm horizontallyand to store electronic components.

1

2

4 3

Figure 17: Support arm with connector panel

1 Control panel [} 61] 2 Suspension arm mount

3 Ventilation opening 4 Connector panel [} 48]


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3.2.13 Integrated 22" monitorThe integrated 22" monitor can be used for dual observation of thesurgical procedure by sterile surgical staff.

1

Figure 18: Integrated 22" monitor

1 Display

3.2.14 Support arm for integrated 22" monitorThe support arm is used to orient the integrated 22" monitor verti-cally or horizontally.

1 2

3

4

Figure 19: Support arm for integrated 22" monitor

1 VESA interface 2 Suspension arm

2 Support arm 4 Holder


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3.2.15 Instrument trayThe instrument tray is intended to hold ZEISS devices.

1 2

Figure 20: Instrument tray

1 Mount for integrated 22"monitor

2 Instrument support

3.2.16 Integrated keratoscope ringThe integrated keratoscope ring provides intraoperative visualiza-tions of corneal curvatures. An elliptical reflection of the kerato-scope ring light on the cornea displays the direction of the astig-matism. The direction provided is merely an indicator for the astig-matism and is not intended for use in measuring the astigmatism'srefractive power.

1

Figure 21: Integrated keratoscope ring

1 LED illumination

The red LED illumination system forms a ring around the objectivelens.


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3.2.17 Connections on the surgical microscope

1

2

3

45

Figure 22: Connections on the surgical microscope

1 Right coobservation output 2 Left coobservation output

3 Light guide input 4 RESIGHT 700 port

5 Invertertube E port

3.2.18 Connections on the assistant's microscope

1

Figure 23: Connections on the assistant's microscope

1 Invertertube E port


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3.2.19 Connector panel

1

2 3 4 5

6

789101112

Figure 24: Connector panel (example with optional connections)

1 USB port for HD video andimage recording (optional)

2 USB service port

3 LAN 1 network connection(optional)

4 Remote connection forexternal devices with amaximum switching capacityof 24 V / 0.5 A.

5 Foot control panelconnection

6 IEC 60601-1 standardpotential equalizationconnector

7 Sliding switch for ratedvoltage

8 Connector panel for theintegrated HD camera(optional)

9 Power outlet with maxvoltage rating 100 - 240 VAC, max 500 VA

10 Power inlet socket

11 Lemo socket for IDIS(optional, only on externalCALLISTO eye Panel PC)

12 LAN 2 network connection(optional)

3.2.20 Connector panel for the integrated HD camera

1 2 3 4 5

Figure 25: Connector panel for the integrated HD camera

1 Composite video output 2 Y/C video output (green)

3 HD-SDI video output 4 DVI-D video output


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5 YPbPr video output

3.2.21 CALLISTO eye Panel PC connector panel (model I)

7891011121314

1 2 3 4 5 6

15

Figure 26: CALLISTO eye Panel PC connector panel (model I)

1 Voltage connection 2 COM port

3 Microphone port 4 USB ports (4x)

5 HDMI port (disabled) 6 HDMI port for IDIS

7 COM port (disabled) 8 VGA port (disabled)

9 Network connection 10 Network connection

11 Speaker port 12 HDMI port (disabled)

13 HD-SDI video output(disabled)

14 HD-SDI video input

15 Y/C video input

3.2.22 CALLISTO eye Panel PC connector panel (model II)

4 9

12

5 7 8 101 2 3 6 11

131415

Figure 27: CALLISTO eye Panel PC connector panel (model II)

1 Y/C video input 2 HD-SDI 1 video input

3 HD-SDI 2 (disabled) 4 Display port

3 Description of the device Instructions for UseOPMI LUMERA 7003.3 Control elements and displays

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5 HDMI 1 port (for IDIS) 6 HDMI 2 port

7 USB ports (4x) 8 LAN 2 network connection

9 LUMERA 700 / hospitalnetwork LAN 1 networkconnection

10 CAN connector

11 Potential equalization 12 Voltage connection

13 WLAN antenna port 14 Microphone port

15 Speaker port

3.3 Control elements and displays

3.3.1 Superlux Eye light source fault signal

1

Figure 28: Superlux Eye light source fault signal

Item Symbol Name Explanation

1 Redsegment

Illuminated red: xenon lamp isdefective. The backup xenon lampis on.

Instructions for Use 3 Description of the deviceOPMI LUMERA 700 3.3 Control elements and displays

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3.3.2 Halogen light source fault signal

1

Figure 29: Halogen light source fault signal


1 Automaticflap

Flap open: halogen lamp isdefective. The backup halogenlamp is on.

3.3.3 LED light source fault signal

1

Figure 30: LED light source fault signal


1 Amber LED Illuminated amber: LED lightsource is defective. Light intensityis 50%. An error message isdisplayed on the control panel.


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3.3.4 Manual mode fault signal

1

Figure 31: Manual mode fault signal


1 Yellow LED Not illuminated: working mode isactivated

Illuminated yellow: manual modeis activated

• Light sources are at mediumintensity

• XY coupling, focus and zoomare inactive

• The filters are in the swiveled-out position

• Control panel is black


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3.3.5 Overhead display

1 3 4

5

7 6

2

Figure 32: Displayable elements on the overhead display


1 "CAUTION" Displays a message on the controlpanel. Once the message iscanceled by the user, the messagedisappears on the control paneland on the overhead display.

2R

Surgeryprofiles

Empty circle: displays createdsurgery profiles. One circle isdisplayed for each surgery profilewhich has been configured for thecurrent user (max 5).

Filled circle: indicates the activesurgery profile.

R: a surgery profile with RESIGHTprofile is active

3 Light sourcelightintensity

Displays the light intensity from5% to 100%.

4 Video status REC OFF: no video recording.

REC ON: video recording isrunning.

REC ON/REC OFF: no integratedHD image and video recordingavailable.

5 Focusposition

Up arrow: focus 40 mm aboveinitial position.

Center arrow: focus at initialposition.

Down arrow: focus 30 mm belowinitial position.


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6 SCI illumi-nation mixratio

Position 1: red reflex illumination100%, surrounding field illumi-nation 0%.

Position 2: red reflex illumination100%, surrounding field illumi-nation 50%.

Position 3: red reflex illumination0%, surrounding field illumination100%.

7 SCI illumi-nationstatus

Empty icon: light emittedgenerates a red reflex.

Icon half filled: light emittedgenerates a red reflex and simulta-neously illuminates thesurrounding area of the patient’seye.

Icon filled: light emitted illuminatesthe entire field of view.

8 Light sourcestatus

Light lamp: light source is on.

Dark lamp: light source is off.

3.3.6 Surgical microscope

1

667 345

2

Figure 33: Control elements on the surgical microscope


1 [OPMI tilt]adjustmentwheel

Tilts the surgical microscope.

2 Securingscrew

Fastens the tubes or accessories tothe surgical microscope.


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3 [Coobser-vationoutput]rotary knob

Switches from left to rightcoobservation output or vice versa.

4 [SCI illumi-nation]rotary knob

In the event of device fault:manually switch SCI illumination.

• Left position: light emittedgenerates a red reflex.

• Right position: light emittedilluminates the entire field ofview

5 [Integratedslit illumi-nator] rotaryknob

In the event of device fault:position split illuminator manually.

• Left position: slit illuminatorfrom the left

• Center position: standardOPMI illumination

• Right position: slit illuminatorfrom the right

6 Handgrips Positions the surgical microscope.Buttons and directions of rotationare freely configurable. [} 76]

7 Zoomadjustmentknob

In the event of device fault:manual zoom.

3.3.7 Assistant's microscope

1

2

4

3

Figure 34: Control elements on the assistant's microscope


1 Securingscrew

Fastens a tube.


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2 [Zoom]rotary knob

Rotate left: largerRotate right: smaller

3 Lockingbutton

Releases the lock on the assistant'smicroscope. The button is alwayslocated opposite the assistant’smicroscope.

4 Focus knob Rotate left: increaseRotate right: decrease

3.3.8 Invertertube E

2

1

2

Figure 35: Control elements on the Invertertube E


1 [Inversion]adjustmentwheel

Switches between "not inverted"and "inverted".

2 [Inter-pupillarydistance]adjustmentwheel

Sets the interpupillary distance.


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3.3.9 Widefield eyepiece

2

1

Figure 36: Control elements on widefield eyepiece

Item Name Explanation

1 Diopter settingring

Compensates for visual defects from -8 dpt to+5 dpt.

2 Eyecup Prevents the entry of scattered light.

3.3.10 Handgrips

2

1

Figure 37: Control elements on the handgrips


1 Left handgrip Positions the surgical microscope. Factorysettings for buttons and directions of rotation[} 73]

2 Right handgrip Positions the surgical microscope. Factorysettings for buttons and directions of rotation[} 74]


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3.3.11 14-function foot control panel

3

1 1 11 2

1 1

Figure 38: Controls on the 14-function foot control panel


1 Buttons Controls device functions (freely config-urable).

2 Rocker switches Control zoom and focus (horizontal andvertical configuration possible).

3 Joystick Adjusts the XY coupling.


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3.3.12 XY coupling

1

2

Figure 39: XY coupling control elements


1 XY resetbutton

Resets functions to their initialpositions.

Not illuminated: the followingfunctions are in their initialposition:

• XY coupling

• Focus (surgical microscope andRESIGHT 700)

• Zoom

• Light source

Illuminated: a function is active.

2 Frictionadjustmentknob

Enables the surgical microscope torotate left or right.


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3.3.13 Suspension arm

1 2 3 4

Figure 40: Control elements on the suspension arm


1 [Releasemagneticbrakes]switchingstrip

Triggers the magnetic brake. Canbe operated by unsterile persons.

2 [Downwardtravel limit]rotary knob

Sets the minimum workingdistance from the surgical field inthe vertical direction.

3 [Fixingsuspensionarmposition]rotary knob

Prevents the suspension arm fromshooting upward or droppingwhen an accessory is beingattached or removed.

4 [Weightbalancing]rotary knob

Serves to balance the surgicalmicroscope.


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3.3.14 Control panel

1

2

3

Figure 41: Control elements on the control panel


1 [Manualmode]switch

Activates manual control.

2 Controlpanel

Controls and configures thesoftware.

3 Powerswitch

Not illuminated: device is off.

Illuminated green: device is on.


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3.3.15 CALLISTO eye Panel PC (model I)

1

2

Figure 42: Control elements on the CALLISTO eye Panel PC (model I)


1 [Power] button Not illuminated:CALLISTO eye Panel PC isnot connected to a powersource.

[Power] button Illuminated green:CALLISTO eye Panel PC ison.

[Power] button Illuminated orange:CALLISTO eye Panel PC isconnected to a powersource.

2 [TouchFunction]button

Not illuminated: touchscreen is activated.

Illuminated: touchscreen islocked.


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3.3.16 CALLISTO eye Panel PC (model II)

1

2

3

Figure 43: Control elements on the CALLISTO eye Panel PC (model II)


1 [Power] button Not illuminated:CALLISTO eye Panel PC isnot connected to a powersource or the main powerswitch is in the off position.

[Power] button Illuminated green:CALLISTO eye Panel PC ison.

[Power] button Illuminated orange:CALLISTO eye Panel PC isconnected to a powersource.

2 [TouchFunction]button

Not illuminated: touchscreen is activated.

Illuminated: touchscreen islocked.

3 Main powerswitch

Turns the CALLISTO eyePanel PC on and off.


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3.3.17 Superlux Eye light source

1

2

Figure 44: Control elements on the Superlux Eye light source


1 [Backupxenon lamp]switch

Switches to the backup xenonlamp.

2 [Open lampmodule]button

Opens the lamp module.

3.3.18 Halogen light source

1

2

Figure 45: Control elements on the halogen light source


1 [BackupHalogenLamp]button

Switches to the backup halogenlamp.

2 [Open lampmodule]button

Opens the lamp module.

Instructions for Use 3 Description of the deviceOPMI LUMERA 700 3.4 Software description

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3.4 Software description

3.4.1 Structure of the operating panelThe displayed elements consist of the operating panel functions.

1

2

3

Figure 46: Structure of the operating panel

Pos. Name Explanation

1 Footer menu Displays the folllowing elements:

• User and OP profile

• Menu

2 Work area Displays the main content of the operating panel.If the work area is not sufficient for display, themain content of the operating panel is displayedon several tabs.

3 Status bar Displays the device status. Tapping displays statusdetails in the workspace, tapping again decreasesthe display.

3.4.2 Bottom barThe bottom bar displays the available storage options and themenu that is currently open.

1 2 3

Figure 47: Bottom bar


1 Back Temporarily saves values.

3 Description of the device Instructions for UseOPMI LUMERA 7003.4 Software description

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2 System Saves device-specific values(e.g. optical settings,pairing, network, etc.)

User name /Start values

Saves user-specific startvalues. (e.g. SCI illumi-nation, zoom, etc.)

User name /Profile name

Saves profile-specific values.(e.g. light on/off, footcontrol panel configuration,etc.)

User name /Profile name

Saving not possible.

Activate Activates the selected userprofile.

3 Optics Menu name Displays the menu that iscurrently open.

3.4.3 Status barThe icons in the status bar provide information about the currentstatus of the device.

1 2 3 4 5

Figure 48: Status bar


1 Light Light on, light intensity in %.

Light Light off, light intensity in %.

2 Magnifi-cation

Displays the total magnification.

3 Recording For integrated HD video and imagerecording: indicates that recordingis in process.

4 Battery Displays the charge state of thebattery in the wireless 14-functionfoot control panel.

5 WLAN Displays the signal strength of theconnection to the wireless 14-function foot control panel.


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3.4.4 Color codeThe button colors provide information about the status of displayelements or the functions they represent.

Button Color Explanation

Gray Locked button.

Light blue Clickable button.

Blue Clicked or active button.

Gray Locked function.

Light blue Deactivated function.

Blue Activated function.

3.4.5 Interactive buttonsThe following table provides descriptions of all interactive buttonsand their functions.

Button Name Explanation

Save Saves the selected element.

Up arrow Increases the value. When thehighest value has been reached,the arrow button is grayed out.

Down arrow Lowers the value. When thelowest value has been reached,the arrow button is grayed out.

Right arrow Increases the value. When thehighest value has been reached,the arrow button is grayed out.

Left arrow Lowers the value. When thelowest value has been reached,the arrow button is grayed out.

Minus Lowers a value in the "Date &Time" menu.

Plus Increases a value in the "Date &Time" menu.

OK Confirms an action.

Close Closes a menu.

Function button Deactivates a function.


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Function button Activates a function.

Add Adds an element.

Delete Deletes a selected element.

Edit Modifies a selected element.

Workflow steps Opens the "Surgery Profiles"menu.

Photo Selects a photo.

Video Selects a video.

Photo capture Takes a photo.

Tip: During video recording, thephoto capture button can betapped to create additionalindividual images. These can alsobe used as markers for skippingthrough the video recording.

Video recording Records a video.

Playback Starts playback.

Pause Pauses playback.

Stop Stops playback.

Fast forward Increases playback speed by 10%with each press.

Fast rewind Decreases playback speed by 10%with each press.

Skip forward Jumps to the next marker duringplayback. If no marker has beenset, the video skips directly to theend.

Skip backward Jumps to the previous markerduring playback. If no marker hasbeen set, the video skips directly tothe beginning.


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3.4.6 Navigation buttonsThe following elements are used for navigating through menus:


Menu button Opens a menu.

Submenu button Opens a submenu.

Selection field Opens a selection list.

Arrow button Scrolls up in a selection list. Whenthe uppermost element has beenreached, the arrow button isgrayed out.

Arrow button Scrolls down in a selection list.When the bottommost elementhas been reached, the arrowbutton is grayed out.

Slider Scrolls up and down in a selectionlist.

Back Navigates to previous menu orsubmenu and temporarily savesthe selected settings.


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3.4.7 Control panel keyboardIf text entries need to be made, a virtual keyboard is displayed onthe control panel with the following input options:

1

6

2

3

45

Figure 49: Control panel keyboard


1 - Text field -

2 - Numerickeypad

Used to input numbers.

3 Delete Deletes the character to the left ofthe cursor.

4 Space key -

5 - ABC keypad Used to input letters.

6 Shift key Switches between upper-case andlower-case letters.


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3.4.8 Settings for daily operation - main menu, tab 1

1 2

3

45

6

Figure 50: Main menu, tab 1


1 User Manages user and surgery profiles.

2 Light Adjusts the SCI illumination andlight sources.

3 Magnifi-cation of theXY focus

Adjusts the following functions:

• Total magnification

• DeepView

• Focusing the surgicalmicroscope

• Positioning the XY coupling

4 Recording Manages patient data. Used forphoto and video capture.

5 AdditionalSettings

Adjusts user-specific settings.

6 Camera Adjusts the integrated HD camera.


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3.4.9 Basic device settings - main menu, tab 2

21

Figure 51: Main menu, tab 2


1 SystemSettings

Adjusts system-specific settings:

• Optics

• Pairing

• Recording

• CALLISTO eye

• Video format

• Versions

• Date & Time

• Export data

• Service PIN

• Lamp service life

2 CALLISTOconnection

Transfers control to the CALLISTOeye Panel PC.


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3.4.10 Factory settings for handgrips and 14-function footcontrol panel

3.4.10.1 Left handgrip factory settings

Figure 52: Left handgrip preconfigured button assignments


A Releasebrakes

Direction ofrotation A

Releases all magnetic brakes andallows the device to be movedalong all axes.

B Releasebrakes

Direction ofrotation B


C No function Button C

D OPMI filter + Button D Moves forward one filter.

E Profile + Button E Moves forward one profile.


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3.4.10.2 Right handgrip factory settings

Figure 53: Right handgrip preconfigured button assignments


A Releasebrakes

Direction ofrotation A


B Releasebrakes

Direction ofrotation B


C SCI position Button C Switches between the threedefined SCI positions.

D SCI + Button D Increases the SCI light intensity.

E SCI - Button E Reduces the SCI light intensity.


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3.4.10.3 Factory settings for 14-function foot control panel

Figure 54: Foot control panel preconfigured button assignments


A Light - Button A Reduces the light intensity of themain light source.

B Light + Button B Increases the light intensity of themain light source.

C SCI position Button C Switches between the threedefined SCI positions.

D No function Button D

E Light On /Off

Button E Activates or deactivates the mainlight source.

F 2nd lightOn / Off

Button F For integrated 2nd light source:activates or deactivates the secondlight source.

KeratoscopeOn / Off

Button F For integrated keratoscope ring:activates or deactivates the kerato-scope ring.

G Zoom + Rockerswitch G

Increases the magnification on thesurgical microscope.

H Focus + Rockerswitch H

Raises the surgical microscopefocus.

I Zoom - Rockerswitch I

Decreases the magnification onthe surgical microscope.

J Focus - Rockerswitch J

Lowers the surgical microscopefocus.


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3.4.11 Configurable assignments for handgrips and the 14-function foot control panel

Area Function Explanation Assignment possible

No function Button is disabled. x x

Light/illumi-nation

Light On / Off Activates or deactivates the main lightsource.

x x

Light + Increases the light intensity of the mainlight source.

x x

Light - Reduces the light intensity of the mainlight source.

x x

SCI + Increases the SCI light intensity. x x

SCI - Reduces the SCI light intensity. x x

SCI position Switches between the three defined SCIpositions.

x x

Left slit Changes between central illumination andslit from the left.

x x

Right slit Changes between central illumination andslit from the right.

x x

Right/left slit Switches between left and right slit. x x

Slit width + Moves forward one slit width on theintegrated slit illuminator.

x x

Slit width - Moves back one slit width on theintegrated slit illuminator.

x x

OPMI filter + Moves forward one filter. x x

OPMI filter - Moves back one filter. x x

Keratoscope On /Off

Activates or deactivates the keratoscopering.

x x

Retina stop Swings the retina protection device intoand out of the surgical microscope’s beampath.

x x

VISULUX left Positions the VISULUX fiber slit illuminatoron the left side.

x x

VISULUX right Positions the VISULUX fiber slit illuminatoron the right side.

x x


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OPMI Focus + Raises the surgical microscope focus. x x x

Focus - Lowers the surgical microscope focus. x x x

RESIGHT focus + For RESIGHT user profile: raises theRESIGHT 700 focus.

x x x

RESIGHT focus - For RESIGHT user profile: lowers theRESIGHT 700 focus.

x x x

Fast focus Moves the surgical microscope max. 40mm upward; if pressed again, themicroscope moves downward.

x x

Reset XY Moves the XY coupling at maximumspeed to its center position.

x x

Zoom + Increases the magnification on thesurgical microscope.

x x x

Zoom - Decreases the magnification on thesurgical microscope.

x x x

Video/Assis-tance

Profiles - Moves one surgery profile back (accordingto order set in working steps).

x x

Profiles + Moves one surgery profile forward(according to order set in working steps).

x x

Start / stoprecording

Starts or stops video recording. x x

Photo Creates a photo. x x

Invert Inverts the image on the video monitorand Invertertube E.

x x


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Other DeepView On / Off Turns the overhead display on or off. x

Release brakes Releases all magnetic brakes and allowsthe device to be moved along all axes.

x

Release vert. brakes Releases only the vertical magnetic brakes. x

Release horiz.brakes

Releases only the horizontal magneticbrakes.

x

Overhead On / Off Turns the depth of field management onor off.

x x

2nd light On / Off Activates or deactivates the second lightsource.

x x

2nd light filter + Moves forward one filter. x x

2nd light filter - Moves back one filter. x x

AUX On / Off Activates or deactivates additional devicesconnected via the remote connector.

x x

Instructions for Use 3 Description of the deviceOPMI LUMERA 700 3.5 Functional description

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3.5 Functional description

3.5.1 Operating conceptIn order to ensure that the optimal device settings are availableduring different surgical phases, different surgery profiles can becreated for each user. The device automatically adds the user'sprofile to a list of working steps. The order of surgery profiles in thelist of working steps can be modified.

The first surgery profile is always activated when the device isstarted or moved out of the park position. If configured accord-ingly, a button on the 14-function foot control panel or thehandgrips can be pressed to switch to the next or previous surgeryprofile in the list of working steps during surgery. This enables theuser to quickly select the optimal device settings during differentphases of surgery.

It is also possible to set a surgery profile for use with the RESIGHT700 fundus viewing system. In this case, the surgery profile isautomatically activated when the RESIGHT 700 is swiveled intoposition. When the RESIGHT 700 is swiveled back out, the nextsurgery profile in the list is automatically activated.

Example: user with three surgery profiles

User"Dr. Mustermann"

Surgery profile "Cataract"

Surgery profile "Retina RESIGHT"

Surgery profile "Retina Contact"

Press "Profile +"

Swivel RESIGHT 700 into position or press "Profile +"

Swivel RESIGHT 700 out of position or press "Profile +"

3 Description of the device Instructions for UseOPMI LUMERA 7003.5 Functional description

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Example: surgery profile configuration options

User "Mustermann"

Device setting Surgery profile for"Cataract surgery"

Surgery profile for"Retina surgery withRESIGHT"

Surgery profile for"Retina surgery withcontact glasses"

Surgery profile name Cataract Retina RESIGHT Retina Contact

Foot control panelconfiguration

• Buttons C and D

• Rocker switches Jand H

Fast focus

Focus +, Focus -

Focus +, Focus -

RESIGHT focus +,RESIGHT focus -

-

Focus +, Focus -

Handgrip configuration Retina stop

Profile +, Profile -

-


-


Camera

• Light measurementmethod

• Brightness

• Chroma

• Peak / Average

Integral

40 - 50 %

+2

7

Integral

70 - 80 %

+2

0

Integral

70 - 80 %

+2

0

Speed (focus, XY, zoom) High Low Low

Total magnification × × ×

Links × × ×

Reset options × × ×

SCI illumination + - -

Overhead display + - -

DeepView + - -

RESIGHT function - + -

2nd light source - + -

Inversion - + -

RESIGHT internal focus - + -

Integrated slit illumi-nation

- - +

x Function is use-specific

+ Function is switched on

- Function is switched off


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3.5.2 SCI illuminationSCI illumination (Stereo Coaxial Illumination) is used for illuminatingthe surgical field and generating a red reflex.

SCI illumination features three preconfigured types of illumination,the mix ratio of which can be retrospectively adjusted.

Function Effect

Red reflexillumination

Light emitted by the surgical microscope is limited toa diameter of approximately 20mm and generates ared reflex which optimally visualizes the structure ofthe patient's eye.

• Red reflex illumination 100%

• Surrounding field illumination 0%

Mixed light: redreflex withsurroundingfield illumi-nation

The light emitted by the surgical microscopegenerates a red reflex and simultaneously illuminatesthe surrounding area of the patient’s eye.



By changing the ratio between red reflex andsurrounding field illumination, you can influence thedepth perception and detail recognition according toyour surgical needs. If you would like to work withone standard setting only for the entire cataractsurgery, we recommend full (100%) red reflex illumi-nation and about 30-50% surrounding field illumi-nation. These values can be adjusted in the startvalues in each user profile and saved; this allowsthem to be activated for each surgery when thesystem is moved out of the park position.

Surroundingfield illumi-nation

Light emitted from the surgical microscope illumi-nates the entire field of view. The red reflex illumi-nation is deactivated.



3.5.3 Main and auxiliary light sourceThe main light source (OPMI light) provides light to the SCI illumi-nation system and is only used for operations on the anteriorsegment of the eye. When working on the posterior segment ofthe eye with Endo illumination, the main light source can beswitched off and the auxiliary light source (2nd light source)switched on. The following functions can be adjusted for both lightsources:


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Function Effect

Light status The following status options are available:

• [On]: OPMI light is switched on followingactivation of the device setting.

• [Off]: OPMI light is switched off followingactivation of the device setting.

• [Standby]: OPMI light is in standby modefollowing activation of the device setting. Onlyavailable if a xenon lamp is installed for the OPMIlight on your device. In standby mode, the lampis switched on, but blocked out. This preventsflickering of the light which occurs on ignition ofthe xenon lamp.

Light intensity The light intensity can only be adjusted for theauxiliary lamp if [On] is selected as the initial state.

Filter The selection of filters depends on which filters areinstalled. It is also possible to select [Without] for nofilter.

3.5.4 Total magnificationThe total magnification is a function of the zoom value and theoptical parameters on the eyepieces, tube and lens. The zoom valueis not directly set on the device; rather, it is adjusted via the totalmagnification settings. When the total magnification is changed,the zoom adjusts so that the device zoom/eyepieces/tube/lensproduce the set total magnification.

3.5.5 Fast focusFast focus is used to quickly switch between two different focuslevels. This might be necessary if IOL is used or an Endo light sensoris implemented. When fast focus is activated, the surgicalmicroscope moves from its current focus position upward andaway from the eye according to the value set (max. 40mm or tothe respective stop). Activating fast focus again returns the focus toits initial position. The focus will not return to its initial position ifthe following actions are performed following activation of fastfocus:

• The device is restarted

• A magnetic brake is released

• The user profile is switched

• The surgery profile is switched

• The XY Reset button is pressed

The "fast focus" function can only be activated by means of the 14-function foot control panel or the handgrips. This requires config-uring the 14-function foot control panel or the handgrips to do so.


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3.5.6 RESIGHT functionsThe device can be equipped with the RESIGHT 500 or RESIGHT 700contact-free fundus viewing systems. The fundus viewing systemprovides a detailed view of the retina without having to move themicroscope. Swiveling the fundus viewing system into the surgicalmicroscope's beam path inverts the microscope image, turning theimage upside down. The Invertertube E can be used toautomatically display the image correctly again. The followingRESIGHT 700 settings can be adjusted for automatic focus andimage inversion:

Function Effect

Invertertube Eimage inversion

Displays the image in an upright position (normal) orinverts it.

RESIGHT 700internal focusspeed

Controls the speed of the RESIGHT 700's internalfocus. The internal focus ensures that the surgicalmicroscope no longer needs to be vertically moved.When working on the anterior segment of the eye,the RESIGHT 700 can be moved out of the beam pathwithout blurring the surgical microscope image.

RESIGHT 700internal focustwo-step speed

Switches the two-step speed on or off.

• If two-step speed is switched off: the devicefocuses using the same speed set by the user.

• If two-step speed is switched on: tapping andholding down the focus setting changes thefocus speed, starting from the smallest speedvalue (factory setting) and then increasing inspeed.

3.5.7 DeepViewDeepView optimizes the depth of field or the light transmission ofthe microscope image.

Function Effect

DeepView isswitched on

Sharp depth perception at every magnification.

DeepView isswitched off

Optimal light transmission for a bright image withhigh resolution.

3.5.8 Reset optionsThe reset options are basic settings that the device reverts back towhen the XY reset button is pressed on the OPMI or the device is inthe park position. The following functions can be adjusted:

Function Effect

Reset XYposition

Moves the XY coupling at maximum speed to itscenter position.


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Function Effect

Reset focusposition

Moves the OPMI focus and internal focus on theRESIGHT 700 fundus viewing system (if connected) totheir initial positions (center position). This settingcannot be deactivated. Hence, the button is alwaysblue.

Reset magnifi-cation to startvalue

Resets the total magnification to its configured startvalue.

Reset illumi-nation to startvalues

Resets the SCI illumination settings and the lightsource brightness to their configured start values. Thefilter selection is not reset to its configured startvalue.

3.5.9 LinksLinks can be used to couple various settings with one another.When one setting is changed, the settings linked to it areautomatically changed as well. The following functions can beadjusted:

Function Effect

Couple lightintensity ofkeratoscope tolight intensity ofOPMI

Couples the light intensity of the keratoscope to theSCI illumination. This link is only available if thekeratoscope ring is installed.

Couple assistantzoom to OPMIzoom

Couples the zoom system of the assistant’smicroscope to the main microscope's zoom system.This link is only available if the assistant's microscopeis installed.

Couple XY andfocus speed tomagnification

Couples the speed of the XY coupling and focus tothe current total magnification value. This link facili-tates focusing on object details, as the presetfocusing speed is automatically reduced at highermagnifications.

3.5.10 Manual modeManual mode switches from working mode to manual mode in theevent of a device fault. In manual mode, the device uses thefollowing settings:

• Light sources are at medium intensity.

• XY coupling, focus and zoom are inactive.

• Filters are swiveled out.

• The control panel is black.

To continue working in manual mode:


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• Manually set the magnification on the microscope's zoomadjustment knob.

• Manually position the suspension system for focusing and formoving the system in the XY direction.

Pressing the manual mode button again switches the device backto working mode.

3.5.11 Assistant's microscopeThe device can be equipped with an assistant's microscope. Theassistant’s microscope is rotatable and has two working positions.These working positions are to the left and right of the mainsurgeon and at a 90° angle. The assistant's microscope can beswiveled out of the 90° position by using the swivel mechanism.The swivel mechanism lock holds the assistant's microscope inposition when the surgical microscope is tilted horizontally. Theassistant’s microscope features a focusing system and is equippedwith a motorized zoom system or a manual 5x magnificationchanger.

No. Function Effect

1 Electrical zoomsystem

The electrical zoom system worksindependently of, or in parallel with, thesurgical microscope zoom feature.

2 Alternative: manual5x magnificationchanger

The manual 5x magnification changerworks independently of the surgicalmicroscope's zoom feature.

3.5.12 IDIS (Integrated Data Injection System)The device can be equipped with IDIS. IDIS enables data to beinjected into the device's right eyepiece or CALLISTO eye.

The following device status information can be displayed:

• Main light source brightness

• Auxiliary light source brightness

• Zoom system magnification

• Charge state of the battery for the foot control panel

• Signal strength of the foot control panel radio connection

Recorded OCT images and the visible area on the screen and in thevideo can be injected from CALLISTO eye.

If CALLISTO eye is equipped with the "Assistance Functions"option, additional assistance functions data can be injected.

• K TRACK : visualization of the shape of the cornea in combi-nation with the keratoscope ring.

• Z ALIGN : an assistance function for aligning toric intraocularlenses.


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• RHEXIS : provides assistance when reaching the desired sizeand shape of the capsulorhexis.

• Incision/LRI : an assistance function for positioning incisions andLRIs.

IDIS can only be configured and activated via CALLISTO eye.

3.5.13 Integrated slit illuminationThe device can be equipped with integrated slit illumination. Theslit illuminator allows you to produce a bright, sharply delimited slitimage for high-contrast observation through the surgicalmicroscope. Due to its fixed illumination angles of +6° or -6°, theintegrated slit illuminator is suitable primarily for retina applicationswith contact glasses. Additional Endo illumination is therefore notnecessary for this purpose. The illumination angle can be controlledusing the configured buttons on the foot control panel, theconfigured buttons on the handgrips, or the control panel. Thefollowing functions can be adjusted:

Function Effect

Status The slit illuminator is switched on or off:

Light intensity The light intensity can only be set when the slit illumi-nator is switched on.

Slit width Available slit widths:

• 0.2 mm

• 2 mm

• 3 mm

• 4 mm

Slit position The slit position can be moved from left to right orvice versa by means of an electric motor.

3.5.14 Integrated HD cameraThe device can be equipped with an integrated HD camera. Defaultsettings can be loaded from the device settings for the integratedHD camera, and settings can be manually adjusted.

The default settings are located in the "Anterior" and "Posterior"surgery profiles. Both default settings have been factory-configuredto optimally adjust the camera to the requirements of the surgicalsituation. The "Anterior" default settings have been optimized forapplications in the anterior segment, the "Posterior" defaultsettings for applications in the posterior segment of the eye.

The user can choose between automatic and manual exposure forboth default settings.


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• Automatic exposure adjusts the brightness of the video imageto the specified nominal value automatically.

• Manual exposure deactivates the exposure metering and sets afixed exposure time.

The following color values can be adjusted for both defaultsettings:

Function Effect

Hue Shifts the entire color spectrum.

Chroma Controls the color saturation. The higher the value isset, the more intense the colors are displayed.

Red and bluevalue

Raising the blue value results in a cold image; raisingthe red value produces a warm image.

Peak / average Influences the characteristics of the automaticexposure. When set to 0, the HD camera adjusts theimage brightness so that the brightest image area isnot distorted. When set to the maximum value (+8),the HD camera sets the brightness to the middlevalue. When set to values between +1 and +7, thebrightness is set to a value between both extremes.

3.5.15 Integrated HD video and image recordingThe device can be equipped with integrated HD video and imagerecording. The integrated HD video and image recording is used foreasy recording of videos and photos in clinical applications. Therecorded videos and photos can be stored on an external USBstorage device or in a shared directory within an IT network. Theunambiguous, automatic storage of videos and photos withtimestamps ensures that they are reliably assigned to the relevantpatient. The integrated HD video and image recording is only usefulwhen used in conjunction with a connected video monitor, as thevideo recording can only be played back on the video monitor. Thefollowing functions can be adjusted:

Function Effect

Auto DeleteMode

When "Auto Delete Mode" is turned on:

• Files older than 3 days are automatically deleted

• Video and photos are not assigned to a patient;rather, they are stored in a neutral folder

Image format Saves recorded photos in TIF or JPG format.

Acousticindication onphotos

Produces an acoustic indication on recorded photos.


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Function Effect

Video quality Saves video recordings at the following quality levels:

• Low - suitable for documentation purposes

• Medium - suitable for documentation purposes

• High - suitable for presentations

Storage location Saves videos and photos to the network or to a USBstorage device.

Video log andOS licenses

Exports video log and OS licenses to the IT networkor to a USB storage device.

Instructions for Use 4 InstallationOPMI LUMERA 700 4.1 Safety during installation

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4 Installation

4.1 Safety during installation

CAUTION! Risk of injury due to electrical current!

Connecting unrecognized, defective or non-permitted accessoriesto live ports may result in electric shock.

u Connect only recognized, functioning and permitted acces-sories to live ports.

u When configuring your ME system, please make sure to complywith the requirements of IEC 60601-1:2005+A1:2012, chapter16.


As per IEC 60601-1, section 16.2, this device's power outlet is amultiple electrical outlet intended for use with an ME system.Connecting unrecognized, defective or non-permitted accessoriescan lead to a reduced level of safety on the ME system.

u Use the multiple electrical outlet only for accessories which arepart of the ME system or are compatible with the ME system.

u Never connect auxiliary power strips or extension cords.

u Do not exceed the maximum permissible electrical load of themultiple electrical outlet.

NOTE Setting up an ME system!

Anyone connecting auxiliary equipment to medical electricaldevices is a system configurer and, as such, is responsible forcompliance of the system with the system standards. Local legis-lation has priority over the above normative requirements.

u Connect only devices which are approved by ZEISS or demon-strably comply with the applicable standards and directives(e.g. IEC 60950:2005 for data processing equipment). Inaddition, all configurations must meet the normative require-ments for medical systems (see IEC 60601-1-1 or Section 16 ofthe 3rd edition of IEC 60601-1).

u If you have any questions, please contact your local dealer orZEISS Service.

4 Installation Instructions for UseOPMI LUMERA 7004.2 Preparing the installation

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4.2 Preparing the installation

4.2.1 Requirements for connecting the device to an ITnetworkThe device can be connected to an existing IT network. Thisenables:

• Video and image data to be saved to a shared directory.

• OPMI LUMERA 700 to be connected to CALLISTO eye. Thisfunction enables the configuration / remote control of variousfunctions of the surgical microscope via the Ethernet interface.

CAUTION! Risk of damage caused by viruses!

Connecting the device to an existing IT network or connecting aUSB storage medium to the device may infect the device withviruses! This may lead to limited functionality or malfunctions in thedevice.

u Keep the IT network or USB storage medium free of viruses.The institution operating the software is responsible for thesafety of the IT network.

CAUTION! Unknown risks due to network integration!

Integration of the device in an existing IT network which includesother ME devices may lead to unknown risks for patients, operatorsor other persons.

u The operator of the device must determine, analyze, evaluateand control these risks before the device is integrated in the ITnetwork.

u The following changes to the IT network can result in new risksand may therefore necessitate additional analyses:- Changing the IT network configuration- Attaching auxiliary elements to the IT network- Removing elements from the IT network- Updating devices which are connected to the IT network

CAUTION! Risk of electric shock!

If the IT network does not provide the features required tointegrate the device into the IT network (listed below), thefollowing hazards may arise:

Risk of electrical shock if the user touches a live part of the casingor a patient.

Increased leakage current on the power outlets.

The following specifications and measures as per IEC 60601 are tobe adhered to when connecting the device to an existing ITnetwork:

Instructions for Use 4 InstallationOPMI LUMERA 700 4.2 Preparing the installation

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• The IT network to which the device is to be connected musthave the following features:

– IPv4, static or dynamic address.

– Any IP address.

• The IT network to which the device is to be connected musthave the following configuration:

– The firewall is open for inbound ports.

– All data is transmitted unsecured from the device to thecustomer's secured internal network.

– No data is transmitted externally from the device.

• Requirements in relation to network connection with thedevice:

– The IT network has a RJ45 network connection, at leastCat.5, 100 Mbit/s.

– The device has a network isolator in compliance with IEC60601-1 which means it is not connected to the IT networkpower supply.

– The operator is responsible for the topology of the ITnetwork, the flow of information and the routing betweenthe device, the IT network and other devices.

4 Installation Instructions for UseOPMI LUMERA 7004.3 Connections

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4.3 Connections

4.3.1 Connecting the power supply

1

230 V

115 V

2

3

Figure 55: Connecting the power supply

1 Sliding switch for ratedvoltage

2 Power inlet socket

3 Potential equalization connector

WARNING! Risk of injury caused by electrical voltage!

u To prevent the risk of electric shock, this device may only beconnected to a power grid which is connected to a flawlessprotective ground conductor.

NOTE Device damage resulting from incorrect rated voltagesetting!

u Check to make sure the rated voltage sliding switch corre-sponds to the rated voltage of the net available at the site ofinstallation.

u If the rated voltage is not correctly set, adjust the sliding switchusing a suitable tool.

Material • Included power cord

Prerequisite þ The power switch is off.

þ The sliding switch's rated voltage corresponds to the ratedvoltage of the net available at the site of installation. Possiblevalues are 115 V / 230 V, 50-60 Hz.

Action 1. Plug the included power cord into the power inlet socket.

2. Plug the power cord into the power outlet.

3. Secure the power cord using the strain relief device [} 104].

4. If required: connect the potential equalization connector to theequipotential bonding bar in the OR.

Instructions for Use 4 InstallationOPMI LUMERA 700 4.3 Connections

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4.3.2 Connecting the 14-function foot control panelThe device can be controlled using either the wireless or wiredvariants of the foot control panel.

4.3.2.1 Connecting the wireless variant

Action 1. Turn on the device at the power switch.

2. Put the 14-function foot control panel in a vertical position inthe immediate vicinity of the device.

3. Run the pairing. [} 140]

4.3.2.2 Connecting the wired variant

1

2

Figure 56: Connector panel

1 Foot control panel connector 2 Foot control panel connector

Material • 3m, 6m or 10m cable

Action 1. Insert the 4-pin connector (straight or angled) into the footcontrol panel port on the suspension system.

2. Insert the 6-pin connector into the foot control panel port onthe 14-function foot control panel.


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4.3.3 Setting up a network connection with the CALLISTOeye Panel PCThe device can be connected either directly (point to point) orindirectly via a switch to an external CALLISTO eye Panel PC. Tip: We recommend establishing a network connection via aswitch. With this configuration you can switch on the devices inany order.

4.3.3.1 Setting up a network connection via a switch

21

3

Figure 57: Network connection with CALLISTO eye Panel PC (model I)

21

3

Figure 58: Network connection with CALLISTO eye Panel PC (model II)

1 LAN 1 network connection 2 Switch

3 LAN 1 network connection


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In the event of a defect in the IT network, the network cable plugcan carry dangerous voltage.

u Check to make sure that the requirements [} 90] for connectingthe device to an IT network are met.

Material • 2x network cable, 10m

Action 1. Turn the device and the CALLISTO eye Panel PC off.

2. Connect the network connections of both devices to theswitch. Cable: 2x network cable, 10 m

3. Turn the switch on.

4. Turn the device and the CALLISTO eye Panel PC on.

5. Configure the network connection with CALLISTO eye. [} 142]


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4.3.3.2 Setting up a direct network connection (without IT networkconnection)

1

2

Figure 59: Network connection with CALLISTO eye Panel PC (model I)

1

2

Figure 60: Network connection with CALLISTO eye Panel PC (model II)

1 LAN 1 network connection 2 LAN 1 network connection

Material • Network cable, 10m

The network connection is established during startup. Thereforeobserve the following steps:

Action 1. Turn the device and the CALLISTO eye Panel PC off.

2. Disconnect the CALLISTO eye Panel PC from the power.

3. Connect the network connections of both devices. Cable:network cable, 10 m

4. Reconnect the CALLISTO eye Panel PC to the power.


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ð The CALLISTO eye Panel PC network adapter is nowactivated and visible for the device.

5. Switch the device on.

6. Turn the CALLISTO eye Panel PC on.


Tip: After each of the network connectors have been unpluggedand plugged back in, the device and CALLISTO eye Panel PC mustbe restarted to adjust to the changes in the network.


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4.3.4 Setting up a network connection with integratedCALLISTO eye Panel PCThe device can be connected either directly (point to point) orindirectly via a switch to an integrated CALLISTO eye Panel PC.

4.3.4.1 Setting up a network connection via a switch

3

2

1

Figure 61: Setting up a network connection via a switch


3 Switch


In the event of a defect in the IT network, the network cable plugcan carry dangerous voltage.

u Check to make sure that the requirements [} 90] for connectingthe device to an IT network are met.

Material • 2x network cable, 10m

Action 1. Switch the device off.

2. Connect the LAN 1 and LAN 2 network connectors to thehospital IT network. Cable: 2x network cable, 10 m

3. Switch the device on.



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4.3.4.2 Setting up a direct connection (without IT networkconnection)

1

2

Figure 62: Setting up a direct connection


Material • Patch cable

Action 1. Connect the LAN 1 network connector to the LAN 2 networkconnector. Cable: patch cable



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4.3.5 Connecting IDIS via CALLISTO eye Panel PCIn order to use IDIS, you must connect the device to the CALLISTOeye Panel PC.

12

3

456

Figure 63: IDIS with CALLISTO eye Panel PC (model I)

12

6 4

3

5

Figure 64: IDIS with CALLISTO eye Panel PC (model II)

1 HD-SDI video output 2 LAN 1 network connection

3 Lemo socket for IDIS 4 HDMI port

5 LAN 1 network connection 6 HD-SDI video input

Material • System cable, Lemo 2B – HDMI, 10m

• HD-SDI video cable 75 Ohm 2xBNC pin, 5mor 10m

• LAN cable, 5m or 10m


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Prerequisite þ To load the assistance functions, a video signal from theintegrated HD camera must be present in the CALLISTO eyePanel PC. Video signals of external cameras are not supportedby CALLISTO eye!

Action 1. Connect the HD-SDI video output to the HD-SDI video input.Cable: HD-SDI video cable 75 Ohm 2xBNC pin, 5m or 10m

2. Connect the Lemo port to the HDMI port. Cable: system cable,Lemo 2B – HDMI, 10m

3. Connect the network connections of both devices. Cable: LANcable, 5m or 10m



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4.3.6 Connecting external video devicesExternal video devices can be connected to devices with anintegrated HD camera. If the device is not equipped with integratedHD video and image recording, you can connect the optionalMEDIALINK 100 SD video recording tool.

4.3.6.1 Connecting the HD monitor to the integrated HD camera

1 2

Figure 65: Connecting the HD monitor

1 HD-SDI video output 2 DVI-D video output


Connecting unrecognized, defective or non-permitted accessoriesto live ports may result in electric shock.

u Connect only recognized, functioning and permitted acces-sories to live ports.

u When configuring your ME system, please make sure to complywith the requirements of IEC 60601-1:2005+A1:2012, chapter16.

Material • System cable DVI-D, 5 m

• Alternative: HD-SDI connecting cable 75 Ohmwith 2x BNC pin

Action 1. Connect the integrated HD camera's DVI-D video output to theDVI-D video input on the HD monitor. The connector side withthe ferrite core must be plugged in on the suspension system.Cable: system cable DVI-D, 5 m

2. Alternative: Connect the integrated HD camera's HD-SDI videooutput to the BNC video input on the HD monitor. Cable: HD-SDI connecting cable 75 Ohm with 2x BNC pin


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4.3.6.2 Connecting the MEDIALINK 100 and SD monitor to theintegrated HD camera

1

2

Figure 66: Connecting the SD monitor via MEDIALINK

1 Y/C video output (green) 2 MEDIALINK 100 connectorpanel

CAUTION! Risk of injury caused by accessories falling down!

If the instrument tray is overloaded or accessories are insufficientlysecured, the risk of injury to the patient is increased.

u Do not exceed the instrument tray’s load capacity of 13 kg.

u Make sure that auxiliary equipment such as the MEDIALINK100 is standing securely on the instrument tray.

u Secure further accessories using the supplied straps.

Material • S video cable out, 10m

• BNC - BNC cable, 10 m

• System cable DVI-D, 5m

Action 1. Connect the integrated HD camera's Y/C video output (green)to the Y/C video input on the MEDIALINK 100. Cable: S videocable out, 10m

2. Connect the MEDIALINK 100's Y/C, BNC or DVI-D video outputto the video input port on your SD video monitor. Cable: seematerials information


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4.3.7 Connecting the strain reliefThe strain relief protects the cables against being pulled out.

Action 1. Form a loop with the cable.Length of cable between strain relief and connector: at least320 mm

2. Open the flap.

3. Push the cable through the opening.

4. Close the flap.

5. Tighten the cable until the flap is enclosed.

6. Check the remaining length of cable between the strain reliefand the connector.

Instructions for Use 5 Daily startupOPMI LUMERA 700 5.1 Outfitting the surgical and assistant's microscopes with accessories

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5 Daily startup

5.1 Outfitting the surgical and assistant'smicroscopes with accessories

5.1.1 Replacing accessories and components

CAUTION! Risk of injury caused by accessories falling down!

Incorrectly mounted auxiliary equipment can fall off and injury thepatient.

u Never replace accessories over the patient.

u Before each use, check to make sure the accessory is mountedfirmly.

u Check to make sure that the securing screws are tight!

CAUTION! Risk of injury caused by lowering of the surgical microscope!

The surgical microscope is not balanced; it can lower and injure thepatient.

u Never replace accessories over the patient.

u Never exceed the device or accessory's maximum permittedweight load.

u Make certain to compensate for any added weight [} 111] tothe device; this will enable the surgical microscope to maintainits balance in all positions of the working range.

u Limit the stroke [} 113] of the suspension arm to prevent anycontact with the patient should the surgical microscope belowered accidentally. This applies in particular during the instal-lation of accessories such as VISULUX or RESIGHT 700.

NOTE Widefield eyepieces with magnetic coupling!

For eyepieces that have been removed from the tube: observe theusual rules for handling magnets.

u Do not place the eyepiece near instruments which may bemagnetizable.

u Do not place the eyepiece on sensitive electronic devices suchas infusion pumps, pacemakers, measuring devices or magneticdata media such as floppy disks, audio and video tapes orcredit cards.

u Always store the eyepiece in its original packaging when notusing it.

5 Daily startup Instructions for UseOPMI LUMERA 7005.1 Outfitting the surgical and assistant's microscopes with accessories

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Material • Tubes and eyepieces for surgical andassistant's microscopes

• Objective lens

• As required: RESIGHT 500 or RESIGHT 700fundus viewing system

• As required: VISULUX auxiliary illuminationsystem or FC oblique illumination system

• As required: coobservation components

Documents • Instructions for Use for the accessory orcomponent

Action 1. Place the suspension arm in a horizontal position. To do this,pull the [Fixing suspension arm position] rotary knob out androtate it 180° to the right or left.

2. Move the suspension arm slightly upward and downward untilthe lock snaps in.

ð Now the suspension arm cannot swing upward.

3. Loosen the securing screw on the main observer and theassistant's microscope a few turns counter clockwise.

4. Remove the dust protection covers and store both of them forlater use.


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5. Attach a tube to the main observer and turn the securing screwclockwise until it is tight. You can install further accessoriesbetween the tube and the main observer in the same way.

6. Attach a tube to the assistant's microscope and turn thesecuring screw clockwise until it is tight. You can install furtheraccessories between the tube and the assistant's microscope inthe same way.

7. Insert eyepieces into the eyepiece mount as far as they will go.When using documentation equipment: insert the eyepieceswith the reticle on the same side of the tube where thedocumentation equipment is located.

ð Magnetic coupling holds the eyepieces.

8. Screw the objective lens into the main observer and tighten it.


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9. Adjust the parameters on the tube, objective lens andeyepieces. [} 139]

10. Additional accessories can be installed on the underside of themicroscope. Refer to the accessory's Instructions for Use.

11. Balance the weight. [} 111]

5.1.2 Connecting the Invertertube EThe electrical inverter on the Invertertube E is controlled by theelectrical connection. If the Invertertube is connected along withthe RESIGHT 700, both accessories are synchronized and the fieldof view is always displayed in the correct orientation. This alsoincludes the image inversion of an integrated HD camera.

Material • Invertertube E connection cable

• Cable clip

Prerequisite þ The Invertertube E is attached.

Action 1. Insert the Invertertube E connection cable into the surgicalmicroscope's Invertertube E connector.

2. For devices with assistant's microscope: follow steps 2 - 8.Insert the Invertertube E connection cable into the assistant'smicroscope's Invertertube E connector.


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3. Secure the connection cable with a cable clip. To do this, pushthe cap out of the cable clip.

4. Form the connecting cable into a loop.

5. Pass the loop through the cable clip.

6. Pull the loop through the cable clip until the connecting cableruns straight upward.

7. Secure the loop in the cable clip. To do this, replace the cap inthe cable clip.

ð The cable clip is secure.


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5.1.3 Connecting RESIGHT 700The RESIGHT 700 internal focus is controlled by the electricalconnection. If RESIGHT 700 is connected along with theInvertertube E, both accessories are synchronized and the field ofview is always displayed in the correct orientation. This alsoincludes the image inversion of an integrated HD camera.

Prerequisite þ RESIGHT 700 is attached.

Action 1. Insert the RESIGHT 700 connection cable into the surgicalmicroscope's RESIGHT 700 connector.

5.1.4 Connecting auxiliary illuminationOn devices with dual light sources, an auxiliary illumination systemcan be connected by means of a second light guide.

CAUTION! Risk of injury caused by suspended light guide!

A suspended light guide may cause retina damage or slight burnsto the patient.

u Always turn off the light source for the light guide that is not inuse.

u Push the light guide that isn't required into a free space on thecable holder so that it is pointing away from the patient.

u Remove the protective cap on the unused light guide. This willprevent melting of the protective cap if the light source isaccidentally turned on.

Material • S light guide, 2.5 m

Prerequisite þ The auxiliary illumination system is attached.

þ The device is switched off.


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Action 1. Insert the end of the light guide as far as it will go into the lightguide socket of the auxiliary illumination system.

5.1.5 Balancing the systemBalancing the weight adjusts the spring force of the suspensionarm so that the surgical microscope remains in position when themagnetic brakes are released.

CAUTION! Risk of crushing caused by moving suspension arm!

Hands and/or fingers can be crushed between the suspension armand the XY coupling.

u Stay clear of the area between suspension arm and XYcoupling while the suspension arm is in motion.

Prerequisite þ A patient is not underneath the surgical microscope.

þ The accessory is attached.

þ The suspension arm is locked in a horizontal position.

Action 1. Roughly balance the weight. Slightly move the arm up anddown while rotating the [Weight balancing] rotary knob.Continue doing this until you feel that sufficient spring force isobtained to compensate for the weight of the surgicalmicroscope and the accessory. To increase the spring force:rotate the [Weight balancing] rotary knob clockwise. Todecrease the spring force: rotate the [Weight balancing] rotaryknob counter clockwise.


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2. Hold the suspension arm in position and gently pull the [Fixingsuspension arm position] rotary knob out. If the rotary knobdoes not release, repeat step 1.

3. Release the magnetic brakes. To do this, press and hold the[Release magnetic brakes] button or the button configured forthis purpose on the surgical microscope handgrip.

4. Move the suspension arm up and down approximately 20 cmwhile adjusting the [Weight balancing] rotary knob until theforce of the upward movement is exactly the same as that ofthe downward movement.

Result ü If the surgical microscope remains in position with themagnetic brakes released, the weight was successfullybalanced.

Instructions for Use 5 Daily startupOPMI LUMERA 700 5.2 Adjusting the surgical and assistant's microscopes

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5.2 Adjusting the surgical and assistant'smicroscopes

5.2.1 Adjusting the downward travel limitThe downward travel limit limits the working distance from thesurgical field. This prevents the surgical microscope from cominginto contact with the patient if it is inadvertently lowered.

Action 1. Release the downward travel limit lock. To do this, rotate the[Downward travel limit] rotary knob counter clockwise.

2. Lower the surgical microscope until you are able to focus whilemaintaining sufficient working distance from the surgical field.To do this, press and hold the [Release magnetic brakes] buttonor the button configured for this purpose on the surgicalmicroscope handgrip.

3. Lock the downward travel limit. To do this, rotate the[Downward travel limit] rotary knob clockwise as far as it willgo.

ð The downward travel limit is set.

4. Check the working distance from the surgical field. To do this,lower the surgical microscope to its lowermost stoppingposition again.

5 Daily startup Instructions for UseOPMI LUMERA 7005.2 Adjusting the surgical and assistant's microscopes

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5.2.2 Adjusting frictionThe friction setting allows the surgical microscope to rotate left andright.

Action 1. To increase mobility: rotate the friction knob counter clockwise.

2. To decrease mobility: rotate the friction knob clockwise.

5.2.3 Positioning the assistant's microscopeThe swivel mechanism allows the assistant's microscope to bepositioned to the left or right of the main observer.

Action 1. Press the locking button and swivel the assistant's microscope abit in the desired direction until the locking position has beenoverridden.

2. Release the locking button and continue to swivel theassistant's microscope until the lock snaps into positionautomatically.

Result ü The assistant’s microscope is secured to prevent it fromswiveling out.


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5.2.4 Adjusting microscope tiltThe manual tilting device can be used to orient the optical axis ofthe surgical microscope vertically to the patient's eye.

CAUTION! Risk of injury caused by assistant's microscope swiveling in!

If you tilt the surgical microscope in the horizontal viewingdirection and the assistant’s microscope is not locked in place, theassistant's microscope may swivel in.

u Position the assistant's microscope and lock it before beginningsurgery.

CAUTION! Risk of injury caused by fundus viewing system swiveling in!

If the RESIGHT 500 or RESIGHT 700 fundus viewing system ismounted on the underside of the microscope, and you steeply tiltthe microscope, the RESIGHT fundus viewing system may swivel in.

u Remove the fundus viewing system before tilting themicroscope at a steep angle.

Action 1. Tilt the surgical microscope towards you: rotate the [OPMI tilt]knob clockwise.

2. Tilt the surgical microscope away from you: rotate the [OPMItilt] knob counter clockwise.

Result ü When the bar on the surgical microscope and that of thesupport arm are perpendicular to each other, the surgicalmicroscope is in the perpendicular position relative to thepatient's eye.

5 Daily startup Instructions for UseOPMI LUMERA 7005.2 Adjusting the surgical and assistant's microscopes

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5.2.5 Adjusting the tubes and eyepiecesWith the right settings, you can achieve an image which is sharplydefined over the complete magnification range without anyrenewed focusing during the magnification setting.

Prerequisite þ The surgical microscope is positioned vertically above a levelobject.

þ Do not wear any bifocal or progressive lenses for theadjustment procedure and subsequent work with themicroscope. Such lenses make correct diopter setting impos-sible and result in unsatisfactory imaging.

þ Have writing implements ready. To permit fast setup of themicroscope, it is advisable to store the pupillary distances andprescriptions of the different users so that they can be easily setduring system preparation.

Action 1. Look through the eyepieces.

2. Position the eyepieces at eye width using the [Interpupillarydistance] adjustment wheel so that both eyepiece imagesappear as a single image.

3. Set the diopter setting on both eyepieces to "0" diopters.

4. Set the surgical microscope to the lowest magnification setting.

5. Look through the eyepieces and move the surgical microscopeto focus the image.

6. Set the microscope to the highest magnification setting andcorrect the image with the focusing function until it is sharplydefined.

7. Reset the microscope to the lowest magnification settingwithout changing the working distance.


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8. Follows steps 9 through 11 for each eyepiece individually.

9. Rotate the diopter adjustment ring on the eyepiece to itsmaximum plus diopter value.

10. Look through the eyepiece.

11. Slowly rotate the diopter adjustment ring in the minus diopterdirection until the image is sharply defined.

ð The microscope generates an image which is sharplydefined over the complete magnification range without anyrenewed focusing while setting the total magnification.

12. Adjust the eyecups so that you can survey the entire field ofview.

ð When viewing with eyeglasses: the eyecups are screwed in.

ð When viewing without eyeglasses: the eyecups areunscrewed.

5.2.6 Adjusting the working distance and magnificationPrerequisite þ The surgical microscope is positioned vertically above a level

object.

Action 1. Focus on the object by moving the surgical microscope.

2. Set the microscope to the highest magnification setting andfocus the image until it is sharply defined.

3. Set the surgical microscope to the required magnification.

ð The focal plane is retained.

5 Daily startup Instructions for UseOPMI LUMERA 7005.3 Positioning the device in the OR

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5.3 Positioning the device in the OR

5.3.1 Moving the device

1

2

3

Figure 67: Moving the device

1 Steerable caster 2 Locking device

3 Transport handle

CAUTION! Risk of injury caused by inappropriate cable routing!

May cause persons to trip and fall.

u Always route cables in a manner such that they do not obstructyour work.

Action 1. Hold the device in position with the transport handle.

2. Unlock all four caster locking devices and carefully move thedevice into a good position.

3. When you have reached the desired position, press the tabs onat least two locking devices.

4. Make sure that the device is standing securely. Push and pullon the transport handle to check.

Instructions for Use 5 Daily startupOPMI LUMERA 700 5.3 Positioning the device in the OR

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5.3.2 Swiveling the device over the surgical field

1

2

3

4

5

Figure 68: Surgical situation (example with an assistant on the left-handside)

1 Support arm 2 Sterilization nurse

3 Surgeon 4 Assistant

5 Suspension arm

CAUTION! Risk of crushing caused by rotating support and suspensionarms!

Fingers may be crushed between the stand column and the supportarm as well as between the support arm and the suspension arm.

u Never touch this area while moving these parts.

Action 1. Swivel the surgical microscope over the surgical field.

2. Bend the suspension arm and support arm to maintain optimalfreedom of movement.


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5.3.3 Placing the device in the working position

1

2

Figure 69: Placing the device in the working position

1 Park position 2 Working position

CAUTION! Risk of injury caused by lowering of the surgical microscope!

If the surgical microscope has not been correctly balanced,unlocking the magnetic brakes may lead to downward movement,causing injury to the patient.

u Only release the magnetic brakes after the system has beenbalanced [} 111] and the surgical microscope remainsstationary in all positions of the working range.

u Check the downward travel limit [} 113] and maintain suffi-cient working distance from the patient. The surgicalmicroscope must not come into contact with the patient even ifit is lowered inadvertently. This applies in particular to installedaccessories such as VISULUX and RESIGHT 700.

u When unlocking the magnetic brakes, hold the system by thehandgrips to prevent it from unintentionally movingdownward.

Prerequisite þ The downward travel limit on the suspension arm is not locked.

Action 1. Release the magnetic brakes.

2. Move the surgical microscope into the desired workingposition.

Tip: An unsterile person can use the switching strip to release themagnetic brakes.

Instructions for Use 5 Daily startupOPMI LUMERA 700 5.3 Positioning the device in the OR

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5.3.4 Orienting the integrated CALLISTO eye Panel PC

1

2

3

Figure 70: Orienting the integrated CALLISTO eye Panel PC

1 Fixing lever 2 Monitor

3 Suspension arm

CAUTION! Risk of crushing caused by moving parts!

Fingers may be crushed between the monitor and support arm.

u Stay clear of the area between the suspension arm and themonitor while the user terminal is in motion.

Action 1. Release the suspension arm by rotating the fixing lever to theright.

ð The suspension arm can be freely moved.

2. Swivel the support arm and the suspension arm into thedesired horizontal and vertical position.

3. Lock the suspension arm by rotating the fixing lever to the left.

ð The suspension arm is locked.

4. Hold on to the upper corner of the user terminal and set thedesired viewing angle.


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5.3.5 Orienting the integrated 22" monitor

1

3

2

Figure 71: Orienting the integrated 22" monitor

1 22" monitor 2 Suspension arm

3 Support arm

CAUTION! Risk of crushing caused by moving parts!

Fingers may be crushed between the monitor and support arm.

u Stay clear of the area between the suspension arm and themonitor while the user terminal is in motion.

CAUTION! Risk of crushing caused by lowering of the 22" monitor!

A loss of gas in the suspension arm may cause the integrated 22"monitor to lower, causing injury to the patient.

u Compensate for the loss of gas by readjusting the gas spring.[} 195]

Action 1. Swivel the support arm and the suspension arm into thedesired horizontal position.

2. Tilt the suspension arm upward or downward until the desiredheight is reached.

3. Hold on to the upper corner of the integrated 22" monitor andset the desired viewing angle.

Instructions for Use 6 Before every useOPMI LUMERA 700 6.1 Safety during preparation

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6 Before every use

6.1 Safety during preparation

WARNING! Risk of injury caused by attached fundus viewing system!



u Prior to using the fundus viewing system, reset the focus.[} 126]

CAUTION! Risk of injury caused by incorrect software settings!

Incorrect software settings may lead to unexpected behavior of thedevice and may cause injuries to the patient.

u Check the selected user before each use.

u Only make changes to your own user profile.

NOTE Loss of functionality caused by hardware or software faults!

u Arrange suitable precautions, irrespective of the application, tobe able to end the operation or application without use of thismicroscope.

u Keep a backup lamp or an OR illuminator ready at hand.

NOTE Light source failure due to overheating!

If the ventilation openings are covered, the device can accumulateheat, and the light source may stop working.

u Never cover any ventilation openings.

6 Before every use Instructions for UseOPMI LUMERA 7006.2 Switching the device on

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6.2 Switching the device on

1

2

Figure 72: Switching the device on (example with integrated CALLISTO eyePanel PC)

1 [Power] button 2 Power switch

CAUTION! Risk of infection caused by particles being stirred up!

The built-in fan can stir up loose particles and transfer germs to thepatient when the device is switched on.

u Only turn the device on when there is no patient beneath thesurgical microscope.

NOTE Device cannot be operated!

The automatic circuit breaker in the power switch was activateddue to a circuit overload or short.

u To switch the device on: press the power switch.

u If the automatic circuit breaker is triggered again, notify ZEISSService.

Prerequisite þ The 14-function foot control panel is connected.

þ For a direct network connection between the device and theCALLISTO eye Panel PC, both devices must be connected bymeans of a network cable.

Action 1. Press the power switch.

ð The power switch will illuminate green and the main menuwill appear on the control panel.

ð The device is ready to be started.

2. If the CALLISTO eye Panel PC is connected: press the [Power]button.

ð The [Power] button will illuminate green.

ð CALLISTO eye is ready for use.

Instructions for Use 6 Before every useOPMI LUMERA 700 6.3 Function test

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6.3 Function testFunction tests reveal faults and incorrect software settings that mayimpact your work or result in unexpected device behavior.

6.3.1 Device function testsUse the following list to check device functionality before each use(patient should not be present!).

Action u Check to make sure all required accessories are attached to thesurgical and assistant's microscopes. [} 105]

ð The surgical microscope can be freely and easily positioned.

u Check to make sure the device weight has been balanced.[} 111]

ð The surgical microscope maintains its balance in allpositions of the working range when the magnetic brakesare released.

u Check to make sure the downward travel limit is set. [} 113]

ð The surgical microscope can be lowered far enough tofocus while maintaining sufficient working distance fromthe surgical field.

u Check to make sure the XY coupling friction is set. [} 114]

ð The surgical microscope is in a fixed position and cannot beinadvertently swiveled to the right or left.

u Check to make sure the surgical microscope is set up. [} 116]

ð Both eyepiece images appear as a single image.

ð The focal plane is retained when zooming.

u Make sure the correct user and surgery profiles are set. [} 132]

ð The saved settings are appropriate for the user.

u Check to make sure the buttons on the 14-function footcontrol panel are configured. [} 147]

ð The device performs the configured functions.

u Check to make sure the handgrips on the surgical microscopeare configured. [} 147]

ð The device performs the desired functions.

u Check to make sure the zoom, focus and XY speeds are set.[} 149]

ð The device moves the components at the desired speeds.

u Check to make sure the SCI illumination system is set. [} 153]

ð The lowest light intensity is set on the device.

ð The desired illumination type is set on the device.

ð A suitable filter is swiveled in on the device.

u Check the light sources. [} 155]

6 Before every use Instructions for UseOPMI LUMERA 7006.3 Function test

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ð For xenon lamps: the remaining service hours must be suffi-cient to complete the operation.

u Check to make sure the objective lens and the eyepieces areclean.

u For integrated IDIS: check the light intensity.

ð The displayed parameters must not blind the user or limitthe field of vision.

u For integrated IDIS: check to make sure the total magnificationis correctly displayed. [} 139]

ð The optical settings match the configuration on the surgicalmicroscope.

u Check to make sure the device is positioned in such a way sothat it can be pushed away from the patient at any time.[} 118]

6.3.2 Function tests for device with fundus viewing systemPrior to using the fundus viewing system, reset the focus.

Action u With the fundus viewing system moved out of the beam path,position the microscope in such a way that the index dot (A) ofthe microscope's focal point is in the middle of the uppertriangle (B).

u Select a medium magnification (i.e. 1.0).

u Lower the microscope to the surgical field until the cornea ofthe patient’s eye is in focus.

u Tighten the [Downward travel limit] rotary knob.

u With no patient present, check to make sure the suspensionarm cannot be lowered any further.

Instructions for Use 6 Before every useOPMI LUMERA 700 6.4 Preparing the system for sterile use

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6.4 Preparing the system for sterile use

6.4.1 Attaching sterile accessories

CAUTION! Risk of infection caused by missing sterile accessories!

The patient or user can become infected if sterile accessories arenot used.

u Use the device only with suitable sterile accessories.

u Disinfect, clean and sterilize sterile accessories before each use.This also applies to the first use after delivery. These proceduresmay only be performed by properly trained personnel.

Material • Sterilizable cap

• Sterilizable cap, 22 mm

• Sterilizable cap, 49 mm

Documents • "Preparation of resterilizable products"manual

Prerequisite þ The resterilizable caps have been sterilized.

Action 1. Slide the sterilizable caps onto the handgrips on the surgicalmicroscope.

2. Turn the sterilizable caps in such a way that the elevations forthe buttons precisely fit on the handgrip buttons.

3. Slide the 22 mm sterilizable cap onto the adjustment knob onthe surgical and assistant's microscopes.

6 Before every use Instructions for UseOPMI LUMERA 7006.4 Preparing the system for sterile use

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4. Slide the 49 mm sterilizable cap onto the [OPMI tilt] adjustmentknob.

5. For 180° tiltable tube: slide the 49 mm sterilizable cap onto the[Interpupillary distance] adjustment knob.

Instructions for Use 6 Before every useOPMI LUMERA 700 6.4 Preparing the system for sterile use

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6.4.2 Placing the drape

1

Figure 73: Placing the drape

1 Objective lens

NOTE Reduced image quality!

Drapes with vision guard may reduce the image quality of theoptics.

u Remove the protective film from the drape lens.

u If the drape lens is dirty, replace it with a new one.

Material • Without camera: drapes (460 mm x 330 mm)

• For 2 observer tubes with camera: sterileOPMI drapes (1220 mm x 2090 mm) or sterileOPMI drapes (1220 mm x 3000 mm)

Action 1. Place the drape on the objective lens. Make sure there is suffi-cient room for the surgical microscope to move.

2. To prevent slippage: secure the drape with the includedadhesive tape.

Instructions for Use 7 OperationOPMI LUMERA 700 7.1 Safety during operation

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7 Operation

7.1 Safety during operation


Contact with plug connector contacts may cause electric shock.

u Never touch the contacts on plug connectors during contactwith the patient.

CAUTION! Risk of injury caused by high IDIS light intensity!

If IDIS is activated, excessive IDIS light intensity in the eyepiece cancause glare and may damage the user’s retina.

u Reduce the IDIS light intensity until an optimum view of thesurgical field is provided.

u If the IDIS light intensity cannot be reduced, deactivate the IDISsystem.

NOTE Loss of functionality caused by hardware or software faults!

The XY movement, focus, zoom, light or magnetic brakes may fail,limiting your ability to operate.


u Contact ZEISS Service.

NOTE 14-function foot control panel failure!

The device cannot be controlled via the 14-function foot controlpanel.

u For wireless 14-function foot control panel: check to make surethe batteries are sufficiently charged.

u If the batteries are charged and the foot control panel does notwork: use the cable to operate the 14-function foot controlpanel.

u If the 14-function foot control panel does not work: activatemanual mode.

7 Operation Instructions for UseOPMI LUMERA 7007.2 Configuring user and surgery profiles

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7.2 Configuring user and surgery profiles

7.2.1 Creating and activating usersUpon first login, the predefined user Default User is set. The DefaultUser cannot be deleted; it features the following characteristics:

• User interface in English

• Anterior surgery profile — for applications in the anteriorsegment of the eye

• Posterior surgery profile — for applications in the posteriorsegment of the eye

Each time the device is started, the previously logged-in user isautomatically activated. The name of the user who is logged in aswell as their surgery profile are displayed below and to the right inthe control panel. A maximum of 40 users can be managed.

Action 1. Open the main menu.

2. Tap the [User] menu button.

ð The user menu will appear.

3. To create a user: tap the button next to the "User"selection field.

ð The screen keyboard will appear.

4. Enter the user name. The name can be no longer than 20characters.

5. Save the user name: tap the button.

ð If the user name does not yet exist, the following messagewill appear: "Which settings should be used?"

6. Assign the settings to [Default User] or [Current User].

7. Save the user. To do this, tap the button.

ð The user will be created and displayed in the selection field.

8. To activate the user: tap the [Activate] button.

Instructions for Use 7 OperationOPMI LUMERA 700 7.2 Configuring user and surgery profiles

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ð A message will appear: "The current user is being changed.Please wait."

Result ü The user is displayed in the footer.

7.2.2 Changing the user languageThe "Default User" language cannot be changed. The followinglanguages can be set for manually added users:

• German

• English

• French

• Spanish

• Italian

• Russian

• Japanese

• Chinese

Prerequisite þ A manually added user is activated.




3. Tap the current language in the "Language" selection field.

ð The selection list will appear.

4. Select the desired user language.

Result ü The selected user language will be changed immediately.

7.2.3 Deleting usersAction 1. Open the main menu.



3. Select an inactive user. The active user and the "Default User"cannot be deleted.

4. Tap the button and confirm the prompt.

Result ü The selected user will be deleted.

7.2.4 Creating a "Cataract" surgery profileThe "Cataract" surgery profile saves device settings [} 79] for appli-cations in the anterior segment of the eye. This surgery profile canbe derived from the preconfigured "Anterior" surgery profile.

Prerequisite þ The user for which the surgery profile is being created is active.




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3. Select the "Anterior" surgery profile. To do this, tap the button next to the "Surgery profile" selection field.


4. Delete the name and replace it with "Cataract". The name canbe no longer than 20 characters.

5. Save the surgery profile. To do this, tap the button.

ð The surgery profile will be created and displayed in theselection field.

6. To activate the surgery profile: tap the [Activate] button.

ð The following message will appear: "The current surgeryprofile settings are being changed. Please wait!".

Result ü The surgery profile is displayed in the footer.

7.2.5 Creating a "Retina RESIGHT" surgery profileThe "Retina RESIGHT" surgery profile saves device settings [} 79]for applications in the posterior segment of the eye with theRESIGHT 500 or RESIGHT 700 fundus viewing system. This surgeryprofile can be derived from the preconfigured "Posterior" surgeryprofile.






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3. Select the "Posterior" surgery profile. To do this, tap the button next to the "Surgery profile" selection field.


4. Delete the name and replace it with "Retina RESIGHT". Thename can be no longer than 20 characters.


ð The surgery profile will be created and displayed in theselection field.

6. To activate the surgery profile: tap the [Activate] button.

ð The following message will appear: "The current surgeryprofile settings are being changed. Please wait!".


7.2.6 Creating a "Retina Contact" surgery profileThe "Retina Contact" surgery profile saves device settings [} 79] forapplications in the posterior segment of the eye with contactglasses. The image inversion and RESIGHT focus functions on the14-function foot control panel can be deactivated. Given the minordifferences between the two profiles, the "Retina Contact" surgeryprofile can be derived from the "Retina RESIGHT" profile.


þ The "Retina RESIGHT" surgery profile has been created andconfigured.





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3. Activate the "Retina RESIGHT" surgery profile.

4. To add the "Retina Contact" surgery profile: tap the buttonnext to the "Surgery profile" selection field.


5. Enter the name "Retina Contact". The name can be no longerthan 20 characters.


ð The following prompt will appear: "Which settings shouldbe used?"

7. To use the active user's current settings: activate the [Currentsettings] button.



7.2.7 Assigning the RESIGHT function to the surgery profileIf a profile features the RESIGHT function designation, and theRESIGHT 700 is swiveled in, the device automatically activates thesurgery profile with the RESIGHT function [} 83].


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2. Open the [User] menu.

3. Tap the button.

ð The "Surgery profile" menu will appear.

4. Select the desired device settings.

ð The selected surgery profile features a light graybackground.

5. Assign the RESIGHT function to the surgery profile. To do this,

tap the button.

ð The selected surgery profile will be designated with an R.

6. To save the settings to a specific user: tap the button.

7.2.8 Configuring working stepsThe order of device settings, and the use of device settings withRESIGHT, can be configured individually for each user.



3. Tap the button.


7 Operation Instructions for UseOPMI LUMERA 7007.3 Device-specific software configuration

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4. Select the device setting you would like to move.

ð The selected device setting features a light graybackground.

5. Adjust the order of device settings with the arrow buttons.

6. To save the settings to a specific user: tap the button.

7.2.9 Deleting a surgery profileAction 1. Open the main menu.


3. Tap the button.


4. Select an inactive surgery profile. The active surgery profilecannot be deleted.

5. To delete the selected surgery profile: tap the button andconfirm the prompt.

ð The surgery profile will be deleted, but will remain in thedevice's internal storage.

6. To delete the surgery profile permanently: Tap the button.

7.3 Device-specific software configurationThis section contains information about user tasks which are notpart of day-to-day operations. These settings apply to all users.

7.3.1 Setting the date and timeThe date and time must be set during the following activities:

• First use

• Change of time zone

Instructions for Use 7 OperationOPMI LUMERA 700 7.3 Device-specific software configuration

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• Switching from summer to winter time, or vice versa

Prerequisite þ No surgical operation is currently in progress. Changing thedate or time requires restarting the device!


2. Tap the [System Settings] menu button.

3. Tap the [Date & Time] submenu button.

ð The configuration menu will appear.

4. Set the desired values.

5. To save the settings for a specific device: tap the [System]button and confirm the prompt.

Result ü The new settings will take effect following restart.

7.3.2 Configuring opticsThe optical parameters must be configured in order to correctlycalculate the total magnification.



3. Tap the [Optics] submenu button.

ð The "Optics" menu will appear.


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4. Select the eyepiece and the objective lens the device is using.

ð Activated functions are illuminated blue.

5. To save the settings for a specific device: tap the [System]button.

7.3.3 PairingWireless operation of the 14-function foot control panel requirespairing it with the device.

Prerequisite þ The foot control panel is in a vertical position and in theimmediate vicinity of the device.



3. Tap the [Pairing] submenu button.

ð The "Pairing" menu will appear.

4. Tap the [Start pairing] submenu button.

ð The following message will appear: "Device and footcontrol panel are being paired".

5. Press any button on the foot control panel until the statusindicator flashes orange. Keep the foot control panel in avertical position. On first-time pairing, it may take up to 20seconds until the radio link between the suspension system andthe foot control panel has been established.

ð The following message will appear: "Pairing successfullycompleted. Place the foot control panel in a horizontalposition and perform a function test. Set the numberspecified on the stand on the rotary wheel of the footcontrol panel."

ð If pairing is successful: the "Radio link intensity" statusindicator will illuminate red for approximately one second,and a message will appear.


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6. Perform a function test. To do this, press any two buttons onthe foot control panel.

ð The "Radio link intensity" status indicator will illuminategreen for approximately one second.

7. Set the number specified on the stand on the rotary wheel ofthe foot control panel.

7.3.4 Configuring the video signal of the integrated HDcamera

7.3.4.1 Configuring the resolution

The resolution can be set to 1080p or 720p.

Prerequisite þ The device includes an integrated HD camera.



3. Tap the [Video format] submenu button.

ð The "Video format" menu will appear.

4. Select the desired resolution.


7.3.4.2 Configuring the display format

If a display device with an aspect ratio other than 16:9 is connectedto the SD output, the display format can be set (letterbox or sidecut). Setting the display format has no effect when using CALLISTOeye for display purposes.

Displayformat

Explanation Image

Letterbox The image will be displayedin 16:9 format, but blackbars will appear at the topand bottom of the screen.

Sidecut The image is cut off on thesides, and only the middleof the image is displayed inan aspect ratio of 4:3. Theblack frame indicates theactual size of the image.




3. Tap the [Video format] submenu button.


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ð The "Video format" menu will appear.

4. Select the desired display format.


7.3.5 Configuring the network connection with CALLISTO eyeThere are two ways to establish a network connection:

• Establishing a network connection with default values [} 142]

• Manually configuring a network connection [} 142]

7.3.5.1 Establishing a network connection with default values

With this function, the device activates the "DHCP" network settingand loads the device and CALLISTO eye data stored in the device.The stored data consists of:

• IP address

• Subnet mask

• Gateway

• Computer name

Prerequisite þ The device is connected to the CALLISTO eye Panel PC via anetwork cable.



3. Tap the [CALLISTO] submenu button.

ð The "CALLISTO eye" menu will appear.

4. Tap the [Reset] button and confirm the prompt.

ð The default network settings will be loaded.

ð The device will restart.

7.3.5.2 Configuring the network connection

The network connection with CALLISTO eye can be configuredmanually or automatically via a DHCP server.

Prerequisite þ The device is connected to the CALLISTO eye Panel PC via anetwork cable.



3. Tap the [CALLISTO] submenu button.

4. Tap the [Network] button.

ð The "Network" menu will appear.


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5. To automatically provide network parameters: activate the[DHCP] button.

ð The button will turn blue.

ð The "IP address", "Subnet mask" and "Gateway" buttonswill become deactivated.

6. To manually input network parameters: deactivate the[DHCP] button.

ð The button will turn light blue.

ð The "IP address", "Subnet mask" and "Gateway" buttonswill become activated.

7. Tap the [IP address] button.


8. Enter the static IP address to be used. Only numeric entrieswith the following syntax are possible:<No.>.<No.>.<No.>.<No.> (ranging between 0 and 255).

9. To save the IP address: tap the button.

ð The "Network" menu will appear.

10. Follow the same steps for "Subnet mask", "Gateway" and"Computer name".


12. Perform a connection test. [} 143]

7.3.5.3 Testing the network connection with CALLISTO eye

Prerequisite þ The CALLISTO eye IP address is known.

þ The "Network" menu is displayed. [} 142]

Action 1. Scroll down using the slider or arrow buttons.

ð The "PING" menu will appear.

2. Tap the [0.0.0.0] button in the "Target IP" field.



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3. Enter the CALLISTO eye IP address. Only numeric entries withthe following syntax are possible: <No.>.<No.>.<No.>.<No.>(ranging between 0 and 255).


ð The "PING" menu will appear.

5. Test the network connection. To do this, tap the [PING] button.

Result ü If the "Ping result - Ping successful" message appears, thenetwork connection was successfully established.

ü If the "Ping result - Ping failed" message appears, thenetwork connection could not be established. There is aproblem with the host address, subnet mask or gateway.Check your host address, subnet mask and gateway.

7.3.6 Configuring integrated HD video and image recordingThe integrated HD video and image recording [} 87] creates HDvideos and photos of the operation.

Prerequisite þ The device includes integrated HD video and image recording.



3. Tap the [Recording] submenu button.

ð The "Recording" menu will appear.

4. Select the desired settings.


Tip: If "Auto Delete Mode" is activated, HD videos and photos olderthan three days will be automatically deleted. Moreover, HD videoand photos are not assigned to a patient; rather, they are stored ina neutral folder. If you would like to assign HD videos and photosto a patient, you must deactivate "Auto Delete Mode".


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7.3.6.1 Configuring the network connection

The network connection for integrated HD video and imagerecording can be established manually or automatically via a DHCPserver.

Prerequisite þ The device is connected to an IT network via a network cable.




4. Tap the [Tab 2] button.


5. Tap the [Network] button. If the button is deactivated, first

activate the [Network] button and then tap the [System]button.

ð The "Network" button will become activated.

ð The "Recording Network" menu will appear.

6. To automatically provide network parameters: activate the[DHCP] button.


ð The "IP address", "Subnet mask" and "Gateway" buttonswill become deactivated.

7. To manually input network parameters: deactivate the[DHCP] button.

ð The button will turn light blue.

ð The "IP address", "Subnet mask" and "Gateway" buttonswill become activated.

8. Tap the [IP address] button.


9. Enter the static IP address to be used. Only numeric entrieswith the following syntax are possible:<No.>.<No.>.<No.>.<No.> (ranging between 0 and 255).

7 Operation Instructions for UseOPMI LUMERA 7007.4 Configuring the software for specific users

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ð The "Recording Network" menu will appear.

11. Follow the same steps for "Subnet mask" and "Gateway".


7.3.6.2 Exporting video logs or OS licenses

Video logs or OS licenses can be saved to an IT network or USBstorage device.

Prerequisite þ A network connection has been established. Alternative: a USBstorage device is connected, recognized and contains sufficientfree storage space.





4. Tap [Tab 2].

5. To export video logs: tap the [Export video log] button.

ð The following message will appear: "Started exporting logfiles. Please wait. Exporting of log files was successful".

ð The generated ZIP archive file contains information aboutthe recorded videos.

6. To export OS licenses: tap the [Export OS licenses] button.

ð The following message will appear: "Started exportinglicenses files. Please wait. Exporting of licenses files wassuccessful".

ð The generated ZIP archive file contains information aboutthe open source licenses used.

7. Close the message. To do this, tap the button.

7.4 Configuring the software for specific usersAll user-specific settings are saved to the user profile or surgeryprofile which is currently active. The existing user profile or surgeryprofile is overwritten (exception: the factory default user is currentlyactive). If you do not want to overwrite the current user profile orsurgery profile, you must first select and activate a different userprofile or surgery profile.

Instructions for Use 7 OperationOPMI LUMERA 700 7.4 Configuring the software for specific users

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7.4.1 Configuring the 14-function foot control panelThe 14-function foot control panel's buttons and rocker switchescan be assigned user-specific functions [} 76]. If the RESIGHT 700 isswiveled in and you would like to control the RESIGHT 700'sinternal focus, the rocker switches must be assigned the followingRESIGHT focus functions:

• RESIGHT focus -

• RESIGHT focus +

Prerequisite þ The surgery profile you wish to configure is activated.

þ In order for the RESIGHT focus functions to be assigned to the"I" and "H" rocker switches, the RESIGHT function [} 136] mustbe assigned to the activated surgery profile.


2. Tap the [Additional Settings] menu button.

3. Tap the [Foot control panel] submenu button.

ð The "Foot Control Panel" menu will appear.

4. Tap the buttons whose assignments you would like to change.

ð The list of available functions will appear.

5. Select the function you would like to assign to the selectedbutton on the 14-function foot control panel.

ð The function will be displayed on the button.

6. To save the changes to the surgery profile: tap the button.

Check the button assignments and functions on the 14-functionfoot control panel before each use and without the patient present.

7.4.2 Configuring the handgripsThe buttons and directions of rotation on the handgrips can beassigned user-specific functions [} 76].



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3. Tap the [Handgrip] submenu button.

ð The "Left Handgrip" menu will appear.

4. To assign a different function to one of the handgrips: tap the"A" or "B" selection field. To assign a different function to one of the buttons: tap the"C", "D" or "E" selection field.

ð The list of available functions will appear.

5. Select the function you would like to assign to the selectedbutton.

ð The function will be displayed on the button.

6. If required: handgrips with different configurations can begiven identical assignments. To do this, tap the [Both] button.

ð Both handgrips will be configured identically.

ð The "Both" button will become grayed out.


Tip: Test the button configuration and the handgrip functionsbefore every use. If the button configuration does not meet yourrequirements, you can reset it to the factory settings.

7.4.3 Configuring image inversion on the Invertertube EDisplays an upside-down image in the correct orientation when theRESIGHT 700 is swiveled in.




3. Tap the [Inversion] submenu button.

ð The "Inversion" menu will appear.


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4. Tap the selection field under "Image orientation".

ð The image statuses will appear.

5. To turn on inversion: tap the [Invert] button.

6. Activate the modified image. Tap the button andconfirm the prompt.


7.4.4 Configuring the direction of the XY couplingIf needed, the direction of the XY coupling can be inverted.




3. Tap the [Inversion] submenu button.

ð The "Inversion" menu will appear.

4. Tap the selection field under "XY direction".

ð The direction will appear.

5. To turn inversion on: tap the [Invert] button.


7.4.5 Configuring speedsThe speeds of the focus, zoom and XY coupling can be setbetween 5% and 100% in 1% increments.




3. Tap the [Speeds] submenu button.

ð The "Speeds" menu will appear.

4. Set the desired speeds.


The speeds of the XY coupling and focus can be coupled with thecurrent total magnification value. The coupling can be activatedand deactivated in the "Links [} 151]" menu.

7.4.6 Configuring the speed of the RESIGHT 700 internalfocusThe speed of the RESIGHT 700 internal focus can be set between10% and 100% in 10% increments.


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3. Tap the [RESIGHT] submenu button.

ð The "RESIGHT" menu will appear.

4. Configure the speed.

5. Activate or deactivate the [Two-step speed] button.



7.4.7 Configuring the overhead displayThe overhead display can be turned on or off. The brightness canalso be set between 0% and 100% in 1% increments. The factorysetting is 50%.


þ The device includes an overhead display.



3. Tap the [Overhead display] submenu button.

ð The "Overhead display" menu will appear.

4. Tap on the [Overhead display On] button to activate ordeactivate the overhead display.


5. Set the desired brightness with the arrow buttons.


Tip: We recommend using a bright overhead display for operationsin the anterior segment of the eye. For operations in the posteriorsegment of the eye, we recommend using a dim overhead displayor turning the display off.

7.4.8 Configuring fast focusFast focus [} 82] is used to quickly switch between two differentfocus levels. The distance can be set between +5 mm and +40 mmin 1 mm increments. The factory setting is +40 mm.


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WARNING! Risk of injury caused by attached fundus viewing system!



u Prior to using the fundus viewing system, reset the focus.[} 126]




3. Tap the [Fast focus] submenu button.

ð The "Fast focus" menu will appear.

4. Set the desired fast focus distance with the arrow buttons.


7.4.9 Configuring linksLinks [} 84] can be used to couple various settings with oneanother.




3. Tap the [Links] submenu button.

ð The "Links" menu will appear.

4. Activate the desired link.


7 Operation Instructions for UseOPMI LUMERA 7007.5 Daily operation

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7.4.10 Configuring reset optionsThe reset options [} 83] are basic settings that the device revertsback to when the XY reset button is pressed on the OPMI or thedevice is in the park position.

CAUTION! Risk of injury caused by lowering of the external focus!

Pressing the XY reset button causes the microscope to focus andlower, which may injure the patient.

u Make sure that the working distance between the microscopeand the patient is greater than the travel range of themicroscope.

Prerequisite þ The user profile you want to configure is activated.



3. Tap the [Reset] submenu button.

ð The "Reset" menu will appear.

4. Activate the desired functions.


5. To save the settings as start values to the user profile: tap the

button.

7.5 Daily operationDuring daily operation, settings can be temporarily adjusted, andcertain settings can be saved to the user profile or surgery profilewhich is currently active.

Instructions for Use 7 OperationOPMI LUMERA 700 7.5 Daily operation

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Doing this overwrites the existing user profile or surgery profile(unless the factory default profile, "Default User", is currentlyactive). If you do not want to overwrite the current user profile orsurgery profile, you must first select and activate a different userprofile or surgery profile.

Temporary settings apply until the settings are modified or any ofthe following actions are performed:

• Restarting the device

• Switching the user profile or surgery profile

• Placing the device in the park position (depending on the resetoptions configuration)

• Pressing the XY reset button (depending on the reset optionsconfiguration)

In all four cases, the microscope reverts to the settings specified inthe selected or active device settings.

7.5.1 Setting the illuminationThe device detects which light source is installed and displays theappropriate settings options. The sections below provide explana-tions of the following light sources:

• SCI illumination

• Main light source (OPMI light)

• Auxiliary light source (2nd light source)

• Integrated keratoscope ring

• Integrated slit illumination

7.5.1.1 Setting the SCI illumination system

The SCI illumination [} 81] system features three adjustable types ofillumination whose mix ratio can be retrospectively adjusted.


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CAUTION! Risk of injury caused by incorrect illumination settings!

Excessive light intensity, long exposure times or using the wrongfilter may lead to retinal damage in the patient’s eye.


u Select an appropriate brightness setting according to therecommended values provided by ZEISS (see "Maximumradiation exposure times" [} 27]). Doing this limits the exposureintensity and the exposure time.

u When operating on the eye, use the retina protection filter. Theretina protection filter protects the patient’s eye from unnec-essary radiation and increases the exposure time.


u Make sure you select the correct filter for the operation.

CAUTION! Risk of injury caused by unsupervised device!

Long radiation exposure times while the device is unattended maylead to retinal damage in the patient's eye.

u If the light source is on: supervise the device.


2. Tap the [Light] menu button.

3. Tap the [OPMI light] submenu button.

ð The "OPMI Light" menu will appear.

4. To set the red reflex illumination: tap the button.

5. To set the mixed light illumination: tap the button.

6. To set the surrounding field illumination: tap the button.

ð The SCI illumination type will be immediately set on thedevice.


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7. If you selected mixed light, use the arrow buttons to modifythe mix ratio.

8. To temporarily save the settings: tap the button.


button.

7.5.1.2 Checking the main and auxiliary light sources

The main and auxiliary light sources [} 81] provide light to the SCIillumination system and the auxiliary illumination system. Beforeeach use, check each light source to make sure it is functioningproperly. The device detects which light source is installed anddisplays the appropriate menu.

CAUTION! Risk of infection caused by xenon lamp rupture!

Lamp fragments may unnoticeably contaminate sterile areas of thedevice.

u Never exceed the lamp's maximum service life of 500 hours.

u When the remaining service life reaches 5 hours, replace thelamp and reset the service hour counter.

NOTE Light source failure caused by ageing of the lamp!

As the light source ages, the actual illumination intensity decreases.The intensity of the light sources may fluctuate, or the light sourcesmay fail.

u Before each use, check each light source to make sure it isfunctioning properly.

u LED light source: If the fault signal is illuminated, the lightsource is defective, and the light intensity is 50%. Inform ZEISSService.

u Xenon light source: If the fault signal is illuminated, the xenonlamp is defective, and the backup xenon lamp is in use. Replacethe lamp.

u Halogen light source: If the fault signal is illuminated, thehalogen lamp is defective, and the backup halogen lamp is inuse. Replace the lamp.

u Keep a backup lamp or an OR illuminator ready at hand.

Action 1. Return to the main menu.


ð The "Light" menu will appear.


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3. Check the remaining service hours.

4. If the remaining service life is less than 5 hours, the backupxenon lamp must be swiveled in and the remaining servicehours reset. [} 193]

7.5.1.3 Setting the main and auxiliary light sources

The following values can be set in 1% increments for the lightsources:

• LED: 2% to 100%

• Xenon: 5% to 100%

• Halogen: 5% to 100%



3. Tap the [OPMI light] submenu button or the [2nd light source]submenu button.

ð The selected submenu will appear.

4. Tab 1: Set the desired light intensity using the arrow buttons.

5. Tab 2: Select an initial state.


7. To save the settings to the surgery profile: tap the button.

7.5.1.4 Setting filters for the main and auxiliary light sources

Filters [} 38] can be swiveled in or out to protect the patient's eye.The filter selection is dependent on the light source installed.



3. Tap the [OPMI light] submenu button or the [2nd light source]submenu button.


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ð The selected submenu will appear.

4. Tab 2: Select a filter.



7.5.1.5 Setting the integrated slit illumination system

The integrated slit illumination [} 86] system generates a high-contrast slit image. An LED light source can be set to valuesbetween 2% and 100% in 1% increments; xenon and halogen lightsources can be set between 5% and 100%.

Prerequisite þ The device includes an integrated slit illumination system.



3. Tap the [Slit] submenu button.

ð The "Slit" menu will appear.

4. To switch on the slit illumination: activate the [Slit On] function.

5. Set the desired light intensity using the arrow buttons.

6. Select the desired slit position.

7. Select the desired slit width.



7.5.2 Setting the total magnificationThe total magnification [} 82] is a function of the zoom value andthe optical parameters on the eyepieces, tube and lens.

Prerequisite þ The optical settings are configured. [} 139]



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2. Tap the [XY focus magnification] button.

ð The "XY Focus Magnification" menu will appear.

3. Set the total magnification with the arrow buttons.

4. To temporarily change the settings: tap the button.


button.

7.5.3 Setting DeepViewDeepView [} 83] optimizes the depth of field or the light trans-mission of the microscope image.



3. Tap [Tab 2].


4. To activate or deactivate depth of field management: tap the[DeepView] button.



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5. To temporarily change the settings: tap the button.


7.5.4 Setting the focus distanceThe focus can be set between -30 mm and +40 mm in 1 mm incre-ments.



3. Tap [Tab 3].


4. Use the arrow buttons to set the focus distance.

ð The selected setting will be immediately applied to thedevice following input.

5. To temporarily save the changes: tap the button.

Tip: If Focus + or Focus - are assigned to one of the buttons, youcan also use a button on the 14-function foot control panel or thehandgrips to change the total magnification.

7.5.5 Changing the XY coupling positionThe XY coupling can be positioned in a 61 x 61 mm area. Thespeed and direction of movement (normal or inverted) can beconfigured.



3. Tap [Tab 3].



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4. Use the arrow buttons to position the XY coupling.

ð The XY coupling will immediately move in the corre-sponding direction. If the video image on the monitormoves in a direction other than indicated on the button,the external video camera needs to be positioned differ-ently.


7.5.6 Setting the integrated keratoscope ringThe integrated keratoscope ring provides intraoperative visualiza-tions of corneal curvatures.

Prerequisite þ The device includes an integrated keratoscope ring.



3. Tap the [Keratoscope] submenu button.

ð The "Keratoscope" menu will appear.

4. To switch on the integrated keratoscope ring: activate the[Keratoscope On] button.


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5. Use the arrow buttons to set the desired light intensity.


7.5.7 Setting the HD DigizoomThe camera image can be digitally magnified from 1.0x to 2.0x in0.1 increments. Digital magnifications do not affect the opticalzoom system.


þ The device includes the CALLISTO eye Panel PC or an integratedmonitor.


2. Tap the [Camera] menu button.

ð The "Camera" menu will appear.

3. Use the arrow buttons to set the digital magnification.

The value set will not be saved. The standard value of 1.0 will bereset after a restart or change of user.

7.5.8 Setting the integrated HD cameraA white balance can be performed to optimize the display of videosand photos. You can still switch between automatic and manualexposure and adjust the color rendering options.

7.5.8.1 White balancing

In the white balance procedure, the system adjusts the HD cameraso that white areas in the surgical field also appear white on thevideo image. This provides a natural color impression when viewingvideos and photos.


þ The surgical microscope is aimed at a white object.

þ The field of view is sharply discernible.


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þ The light source is on.

þ The filters are swiveled in or out.

þ IDIS is off.




3. Tap on the [White Balance] button.

ð The following message will appear: "Please place a whitesheet of paper under the microscope, focus the image, thenpress 'Continue'!"

4. To start the white balance: tap the [Continue] button.

ð The following message will appear: "Please wait - whitebalance in progress!"

ð If the white balance was successful, the following messagewill appear: "White balance successfully completed”.

ð If the white balance fails, the following message willappear: "White balance failed".

5. If the white balancing was successful, tap the button.

Result ü White balancing settings are profile-specific.

7.5.8.2 Setting automatic exposure control

Automatic exposure automatically adjusts the brightness of thevideo image to the specified nominal value. The following lightmetering methods can be set for automatic exposure:

Parameter Symbol Effect

Integral Default. The exposure is measuredover the entire video image. Thislight metering method is recom-mended for surgical fields that arefully and evenly lit.


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Parameter Symbol Effect

Large spot The exposure is measured in anarea in the image center. This lightmetering method is ideal forsurgical fields with darkenededges.

Small spot The exposure is measured in a verysmall area in the image center.This light metering method issuitable for working with anextremely small illuminated fielddiameter. If the object you areinterested in viewing is not locatedin the center of the image, set thelight metering method to "Largespot" or "Integral".




3. Tap [Tab 2].


4. To set the automatic exposure: deactivate the [Manualbrightness] button.

ð The light metering methods will be activated, and"Brightness" will be written in the left values range.

5. Select the desired light metering method.

6. Under "Brightness", set the desired brightness.




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7.5.8.3 Setting manual exposure control

Manual exposure deactivates the exposure metering and sets afixed exposure time. The exposure time can be set to any valuebetween 1/10000 s and 1/8 s. An exposure time in the rangebetween 1/50 and 1/30 usually provides optimum exposure results.




3. Tap [Tab 2].


4. To set the manual exposure: activate the [Manual brightness]button.

ð The light metering methods will be deactivated, and"Exposure time" will be written in the left values range.

5. Under "Exposure time", set the desired exposure time.



7.5.8.4 Configuring color values


þ A white balance was performed. [} 161]




3. Tap [Tab 2].

4. Use the arrow buttons to change the color values for Hue andChroma.

5. Tap [Tab 3].


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6. Use the arrow buttons to change the color values for Redvalue, Blue value and Peak / Average.



7.5.9 RecordingA patient file must first be created and selected before HD videosand photos can be recorded for the first time. Recorded HD videosand photos are automatically allocated to the selected patient file.

7.5.9.1 Creating and selecting a patient file

NOTE Loss of data!

USB storage devices are not suitable for storing patient data longterm.

u Have USB storage devices checked to make sure they are ingood working order before using them.

u Arrange for data to be backed up on a regular basis by your ITadministrator.


þ An IT network or USB storage device is configured to be usedas the storage location. Both devices have sufficient storagecapacity.


2. Tap the [Recording] menu button.


3. Tap the [Change] button next to the patient file.

ð The "Patient" menu will appear.


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4. If required: create a patient file. To do this, tap the button.


5. Create a patient file under the last and first name of thepatient. The name can be no longer than 20 characters.

6. Save the patient file: tap the button for the currently loadeduser.

ð The "Patient" menu will appear.

7. Select a patient file. To do this, tap the button.

8. Load the selected patient file. To do this, tap the button.

Result ü The patient file will be displayed in the "Recording" menu.

7.5.9.2 Recording HD video

NOTE Loss of data!

Removing a USB storage device while data is being saved maycause the data to be lost.

u Never remove USB storage devices while data is being saved.


þ To allocate HD videos to a patient file, "Auto DeleteMode" [} 144] must be deactivated and a patient file [} 165]must be selected.





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3. Start the video recording: tap the button.

ð "REC" will appear in the status bar. The date and time arenot displayed while video recording is in progress.However, this information is recorded and subsequentlydisplayed during playback.

ð The "Change" buttons will become deactivated.

4. Stop the video recording: tap the button.

ð "REC" will disappear from the status bar.

ð The "Change" buttons will become activated again.

Tip: You can use the button to take additional photos duringvideo recording. These photos can also be used as markers. Duringplayback of the HD video, the marked locations can be jumped to

in succession via the and buttons.

7.5.9.3 Taking photos

NOTE Loss of data!

Removing a USB storage device while data is being saved maycause the data to be lost.

u Never remove USB storage devices while data is being saved.


þ To allocate HD videos to a patient file, "Auto DeleteMode" [} 144] must be deactivated and a patient file [} 165]must be selected.





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3. Take a photo: tap the button.

ð The photo will be saved.

ð You will hear an acoustic signal.

7.5.9.4 Viewing HD videos

CAUTION! False diagnosis due to video images!

The monitors are neither calibrated nor designed for diagnosticpurposes. Visualized images may contain variations in shape,contrast and color.

u Do not use the video sequences, video clips (cut sequences) orphotos for diagnostic or treatment purposes.


When viewing or deleting video recordings during surgery, thedevice cannot be operated!

u Do not edit, delete or view any video recordings while thedevice is being operated.


þ The device includes an integrated 22" monitor or an externalmonitor.

þ A patient file has been selected. [} 165]





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3. Open the file directory. To do this, tap the [Change] button.

ð The file directory will open and the available HD videos andphotos will be displayed.

4. Select an HD video. To do this, tap the button.


5. Return to the "Recording" menu. To do this, tap the button.

ð The "Recording" menu will appear and the "Playback"button will be active.

6. To play an HD video: Tap the button.

7. To fast forward or fast rewind through an HD video: tap the

or buttons.

8. To skip to the beginning or end of an HD video: tap the or

buttons.

9. To stop playback of the HD video: tap the button.


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7.5.9.5 Viewing photos

CAUTION! False diagnosis due to video images!

The monitors are neither calibrated nor designed for diagnosticpurposes. Visualized images may contain variations in shape,contrast and color.

u Do not use the video sequences, video clips (cut sequences) orphotos for diagnostic or treatment purposes.


þ The device includes an integrated 22" monitor or an externalmonitor.





3. Open the file directory. To do this, tap the [Change] button.

ð The file directory will open and the available HD photos andvideos will be displayed.

4. Select a photo: tap the button.


5. Return to the "Recording" menu. To do this, tap the button.

ð The "Recording" menu will appear and the button willbe active.


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6. To view a photo: Tap the button.

7. To switch between photos: tap the or buttons.

8. To skip to the first or last photo: tap the or buttons.

9. To stop viewing photos: tap the button.

7.5.9.6 Deleting HD videos or photos


When viewing or deleting video recordings during surgery, thedevice cannot be operated!

u Do not edit, delete or view any video recordings while thedevice is being operated.







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3. Tap the [Change] button to the right of the file.

ð The file folder will appear.

4. To delete an HD video: tap the button. To delete a photo:

tap the button.


5. To delete the file: tap the button and confirm the prompt.

Result ü The file is deleted!

7.5.10 Transferring control to CALLISTO eyeControl of the device can be transferred to CALLISTO eye. Thisenables the device to connect to CALLISTO eye and enables variousfunctions on the surgical microscope to be configured / controlledremotely via the Ethernet interface.

NOTE Unintentional movement during surgery!

Any change in the focus and zoom setting via CALLISTO eye maylead to unintentional movement during surgery.

u Only personnel who have been appropriately trained areallowed to control the surgical microscope via CALLISTO eye.

NOTE Network faults!

Network faults can overload the device and prevent it from beingused.

u End control of the device via CALLISTO eye. [} 173]

u Disconnect the device from the IT network: to do this, unplugthe network cable on the device.

Prerequisite þ The device includes CALLISTO eye.

þ The network connection to CALLISTO eye is configured.



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2. Tap the [CALLISTO Connection] menu button.

ð The "CALLISTO eye" menu will appear.

3. To transfer control to CALLISTO eye: tap the [Allow] button.

ð The following message will appear: "Info - The system isenabled for remote control / Active connection x.x.x.x."

Result ü The control panel is locked. The device can only beoperated via the 14-function foot control panel, thehandgrips and the CALLISTO eye Panel PC.

7.5.11 Ending control via CALLISTO eyeThe network connection to CALLISTO eye can be ended to returncontrol to the device.

Prerequisite þ Control of the device has been transferred to CALLISTO eye.[} 172]

Action 1. Tap the [Disconnect] button.

ð The following message will appear: "Connection toCALLISTO eye terminated. Current user data are beingloaded."

Result ü The user that was active on the surgical microscope beforethe network connection was established will become activeagain on the surgical microscope.

ü Any change of user performed on CALLISTO eye is notapplied.

7 Operation Instructions for UseOPMI LUMERA 7007.6 Typical operating sequence

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7.6 Typical operating sequence

7.6.1 Starting work


If the foot control panel buttons are pressed unintentionally, theexternal focus of the surgical microscope may be lowered andinjure the patient.



Pressing the XY reset button causes the microscope to focus andlower, which may injure the patient.


CAUTION! Risk of infection caused by non-sterile parts!

Unsterile parts may cause injury to the patient.

u Never touch the unsterile connection cable on the assistant'smicroscope while operating the handgrips or zoom button.

Action 1. Turn on the device at the power switch.

2. Check the device for proper function. [} 125]

3. Adjust the tube and eyepieces. [} 116]

4. Swivel the surgical microscope over the surgical field. [} 119]

5. Bring the surgical microscope into its working position. [} 120]

6. Reset the device to its start values. To do this, press the [XYreset button] on the XY coupling. The executed functionsdepend on the configured reset options. [} 152]

7. Look through the eyepieces and lower the surgical microscopeusing the suspension arm until the surgical field comes intofocus.

ð This will allow you to achieve a rough focus.

8. Look through the eyepieces and activate the focusing functionon the 14-function foot control panel or on the handgrip untilthe image of the surgical field appears sharply focused.

Instructions for Use 7 OperationOPMI LUMERA 700 7.6 Typical operating sequence

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7.6.2 Carrying out the working steps

User"Dr. Mustermann"

Surgery profile "Cataract"

Surgery profile "Retina RESIGHT"

Surgery profile "Retina Contact"

Press "Profile +"

Swivel RESIGHT 700 into position or press "Profile +"

Swivel RESIGHT 700 out of position or press "Profile +"

Figure 74: Carrying out the working steps (example)

Prerequisite þ A surgery profile has been created for each phase of surgery.

þ The sequence of surgery profiles has been configured.

Action 1. If you have not already done so, swivel the device into itsworking position.

ð The "Cataract" surgery profile will become activated.

2. Conduct a cataract surgery.

3. To conduct a retina surgery with RESIGHT 700: swivel theRESIGHT 700 into position.

ð The second surgery profile will become activated.

ð The device will load the device settings saved to the surgeryprofile.

4. To conduct a retina surgery with contact glasses: swivel theRESIGHT 700 out.

ð The third surgery profile will become activated.

ð The device will load the device settings saved to the surgeryprofile.

5. Following the operation, if you would like to return to the firstsurgery profile: press the configured "Profile +" button on thehandgrip or the 14-function foot control panel.

Result ü The first surgery profile will become activated again.

Device settings such as illumination, focus and total magnificationcan be changed during the individual phases of surgery. Dependingon the configuration you are using, this can be done via the 14-function foot control panel, the handgrips or the control panel.

7.6.3 Stopping workAction 1. Swivel the surgical microscope into the park position [} 120].

7 Operation Instructions for UseOPMI LUMERA 7007.7 Switching the device off

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ð Depending on how the reset options [} 152] areconfigured, certain functions will be reset to their startvalues.

2. Switch the device off.

7.7 Switching the device off

1

2

Figure 75: Switching the device off (example with integrated CALLISTOeye Panel PC)

1 [Power] button 2 Power switch

Action 1. For an external CALLISTO eye Panel PC: press the [Power]button.

ð The "Power" button will go out.

ð The CALLISTO eye Panel PC is switched off.

2. Press the power switch.

ð The power switch will go out.

ð The device is switched off.

Instructions for Use 8 Cleaning and disinfectionOPMI LUMERA 700 8.1 Safety during cleaning and disinfection

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8 Cleaning and disinfection

8.1 Safety during cleaning and disinfection

Contamination of the deviceDust can penetrate into the internal optics of the device or itsindividual components.

Action u Never shut down the device without objective lens, binoculartube and eyepieces.

u Always store objective lenses, eyepieces and accessories indust-free cases when they are not being used.

u After use, cover the device to protect it from dust.

8.2 Cleaning

8.2.1 Cleaning optical surfacesThe multilayer T* super anti-reflection coating of the opticalcomponents (e.g. eyepieces, objective lenses) ensures optimumimage quality. Even slight contamination or a single fingerprintreduces image quality. Clean the outer surfaces of optical compo-nents (eyepieces, objective lenses) only as required:

Action u Do not use any chemical agents.

u Use a clean and grease-free brush to remove dust.

TIP: For regular cleaning of the surgical microscope’s objectivelenses and eyepieces, we recommend using the optics cleaning kitavailable from ZEISS (Order no.: 1216-071).

8.2.2 Cleaning mechanical surfacesAll mechanical surfaces of the system can be cleaned by wipingthem with a damp cloth.

Action u Do not use any aggressive or abrasive cleaning agents.

u Remove any possible residue using a mixture of 50% ethylalcohol and 50% distilled water plus a dash of householddishwashing liquid.

8.2.3 Fogging of optical surfacesWe recommend using an anti-fogging agent to prevent fogging ofoptical surfaces. Anti-fogging agents like the ones offered byopticians for applications with eyeglasses are also suitable foroptical surfaces from ZEISS.

Action u Observe the Instructions for Use pertaining to the anti-foggingagent concerned.

8 Cleaning and disinfection Instructions for UseOPMI LUMERA 7008.3 Disinfection

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An anti-fogging agent does not ensure fog-free eyepiece optics. Itcleans eyepiece optics and protects them against dirt, grease, dust,lint and fingerprints.

8.3 Disinfection

8.3.1 Disinfection of surfacesThe maximum application concentrations are:

• For alcohol (tested with isopropyl alcohol): 60%

• For aldehyde (tested with glutaraldehyde): 2%

• For quaternary compounds (tested with DDAC): 0.2%

NOTE Surface damage caused by wrong disinfectants!

Performing disinfection with the wrong disinfectants may result indamage to the surfaces of the device.

u Use an aldehyde and/or alcohol-based disinfectant. Theaddition of quaternary compounds is acceptable.

u In order to prevent surface tensions, you may use only thedisinfecting components specified above.

Action u Disinfect all of the required surfaces.

Instructions for Use 9 MaintenanceOPMI LUMERA 700 9.1 Maintenance schedule for the operator

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9 Maintenance

9.1 Maintenance schedule for the operator

9.1.1 Every six months

Component Activity

Manual mode u Check the following functions:

• The light sources are at mediumintensity

• The XY coupling, focus and zoommotor are inactive

• The filter is swiveled out

• The control panel is black

9.2 Maintenance schedule for the authorizedservice

9.2.1 Every six months

Component Activity

Manual mode u Check the following functions:

• The light sources are at mediumintensity

• The XY coupling, focus and zoommotor are inactive

• The filter is swiveled out

• The control panel is black

9.2.2 Every twelve months

Component Activity

Documentation and identifi-cation labels

u Check that the Instructions for Useand identification labels arecomplete, undamaged and legible.

Handles and XY coupling u Check the following functions:

• The visual and acoustic signals arefunctional.

• Manual mode is functional.

• The bearings, stops and suspensionmountings are free of play.

9 Maintenance Instructions for UseOPMI LUMERA 7009.2 Maintenance schedule for the authorized service

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Component Activity

Support system andmicroscope suspensionmounting

u Check the following functions:

• The bearings, stops and suspensionmountings are free of play.

• Brakes are operational at maximumpermissible OPMI configuration.

Stand column u Check to make sure the columnconnection is free of play.

Casters u Check the following functions:

• The casters are free from backlash.

• The casters turn and roll withoutjamming.

• The brakes and locking devices holdsecurely.

• The cable guards are present.

Light sources u Check to make sure the fan is suffi-ciently powerful.

Microscope u Check to make sure the opticalimaging is in good working orderand the field of view is well illumi-nated.

Zoom, focus and illuminatedfield diaphragm


• The zoom system is runningsmoothly.

• The focus, zoom and illuminatedfield diaphragm can be easily moved.

Accessories such as theobjective lens, tube, etc.


• The accessories are free ofmechanical play.

• The accessories are secured withthumb screws.

Wireless 14-function footcontrol panel

u Check to make sure the dust andspray water protection device isundamaged.

u Change the batteries in the 14-function foot control panel.

Integrated 22" monitor u Check the following functions:

• The housing is undamaged.

• The image quality is OK.

• The suspension arm and the gasspring hold the 22" monitor in thedesired position.

Instructions for Use 9 MaintenanceOPMI LUMERA 700 9.3 Performing safety inspections

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9.2.3 Every two years

Component Activity

Light guide u Check to make sure:

• The light guide is intact.

• The light field is uniform.

Light source Check to make sure the light sourcefilters are intact.

9.2.4 Every four years

Component Activity

Support system andmicroscope suspensionmount

u Check to make sure the followingcomponents are free of abrasionand damage:

• Supporting structures

• Interfaces

• Couplings

• Connection and fastenings of thespring assemblies

Cables, plugs and switches u Check the following functions:

• The insulation and plug connectionsof the cables and the device areintact.

• The cable routing and cablefastenings are tight.

Electronics: u Replace the internal batteries.

Casters u Replace the casters.

Light guide u Replace the light guide.

9.2.5 Every six years

Component Activity

Integrated 22" monitor u Replace the support arm, includingthe gas spring.

9.3 Performing safety inspectionsThe safety inspection serves to determine and evaluate devicesafety. The user of this device is obligated to perform anddocument safety inspections in compliance with IEC 62353.

9 Maintenance Instructions for UseOPMI LUMERA 7009.3 Performing safety inspections

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CAUTION! Risk of injury without safety inspection!

Hazards and device deficiencies will not be detected in time andcan have a negative effect on patients, users, or others.

u Have a safety inspection in compliance with IEC 62353performed on time and to the prescribed extent. At the sametime, be sure to observe the relevant national regulations.

Prerequisite þ Only the manufacturer or qualified persons may perform safetyinspections.

Action u Check to make sure the Instructions for Use are available.

u Check to make sure all marks and inscriptions on the device arelegible.

u Check the leakage current and the protective groundconductors.

u Check to make sure the casters and locking devices functionproperly and are not worn-out.

u Perform a function check of all switches, buttons, sockets andindicator lamps of the system.

u Check every six months to make sure manual mode is working.

Instructions for Use 10 TroubleshootingOPMI LUMERA 700 10.1 Localizing malfunctions

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10 Troubleshooting

10.1 Localizing malfunctionsIf a malfunction occurs, the corresponding information is displayedon the touchscreen in the form of a message.

Malfunctions are saved to a log file which can be exported andforwarded to ZEISS.

10.1.1 Response to faults with messagesAction 1. Check the message.

2. Once you have dealt with the issue, tap the message to removeit from the display.

ð The message is saved to a log file and can be exported.

3. If the problem persists, export the log file and send it toZEISS Service.

10.1.2 Exporting log files

1

Figure 76: Exporting log files

1 USB service port

NOTE Connecting USB hubs with power supply!

Connecting USB hubs with power supply to the USB service portcan prevent the device from starting properly.

u USB hubs with power supply must not be connected to theUSB service port.

Action 1. Connect a USB storage device to the USB service port.

2. Open the main menu.


ð The "System Settings" menu will appear.

4. Tap the [Export data] button.

ð The log file is copied to the USB storage device.

10 Troubleshooting Instructions for UseOPMI LUMERA 70010.2 Faults (with messages)

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ð If no USB storage device is connected, the following errormessage will appear: "Error - USB storage medium notfound."

10.2 Faults (with messages)Message / Fault Cause Remedy

Pairing could not be performedsuccessfully. Several foot controlpanels were detected.

Multiple foot control panelsare nearby.

u Restart the pairing process.

Pairing could not be performedsuccessfully. No foot control panelwas detected.

The 14-function foot controlpanel was not in a verticalposition and in the immediatevicinity of the device.

u Place the 14-function footcontrol panel in a verticalposition in the immediatevicinity of the device (less than1m away) and restart thepairing process. In the event ofmalfunction, you can always usethe 14-function wireless footcontrol panel with a cable. Keepthe cable in the vicinity of thesuspension system for this case!

XY coupling error. The error can beacknowledged. If the error impairsyour work, please switch to manualmode and contact your ZEISS servicerepresentative.

Hardware error in motorelectronics

Software error, inadmissiblestatus of motor control

u If the error impairs your work:Activate manual mode.

Light source error. The error can beacknowledged. If the error impairsyour work, please switch to manualmode and contact your ZEISS servicerepresentative.

Malfunction of light intensitysetting

u If the error impairs your work:Activate manual mode. [} 184]

Zoom error. The error can beacknowledged. If the error impairsyour work, please switch to manualmode and contact your ZEISS servicerepresentative.

Jammed hardware u If the error impairs your work:Activate manual mode. [} 184]

Focus error. The error can beacknowledged. If the error impairsyour work, please switch to manualmode and contact your ZEISS servicerepresentative.

Focus system motor is jammed u If the error impairs your work:Activate manual mode. [} 184]

Error during system start. Pleasereboot the system, making sure thatno function buttons are pressedduring the booting process.

A button was pressed duringsystem start.

u Restart the system. Make surenot to press any buttons duringthis process.

Instructions for Use 10 TroubleshootingOPMI LUMERA 700 10.3 Faults (without messages)

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Message / Fault Cause Remedy

System error. The error can beacknowledged. If the error recurs,please contact your ZEISS servicerepresentative.

Unknown software orhardware error.

u Acknowledge the errormessage.

u If the message appears again,contact ZEISS Service.

10.3 Faults (without messages)

10.3.1 Device faults

Fault Cause Remedy

No electrical function in device The power plug is not pluggedin.

u Connect the power plug. [} 92]

The stand power switch is notswitched on.

u Check to make sure the powerswitch is illuminated green. If itis not: press the power switch.[} 124]

Automatic circuit breaker inthe stand power switch isbeing triggered.

u Press the power switch. [} 124]

u If the automatic circuit breakeris triggered again, notify ZEISSService.

There is a power supply failure. u Contact the in-house electrician.

Illumination on the surgicalmicroscope is out of service.

Suspension arm is in the parkposition.

u Move suspension arm into theworking position. To do this,pull the suspension armdownwards. [} 120]

The light source is notswitched on.

u Press the configured buttons onthe handgrip or the 14-functionfoot control panel.

Halogen light source: halogenlamp failure.

u Switch halogen lamps. [} 192]

Superlux Eye light source:xenon lamp is defective.

u Swivel the backup xenon lampin. [} 193]

Superlux Eye light source:xenon lamp and backup xenonlamp are defective.

u Change the Superlux Eye lightsource lamp module. [} 194]

Superlux Eye light source: lampmodule is not making contact.

u Push the lamp module in as faras it will go. [} 194]

Light guide is not properlyinserted on the microscope.

u Push the light guide in as far asit will go.

Stand electronics failure. u Illuminate the OP field with anOP lamp.


10 Troubleshooting Instructions for UseOPMI LUMERA 70010.3 Faults (without messages)

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Fault Cause Remedy

Illumination on the surgicalmicroscope is faulty.

Brightness level set too low. u Increase the brightness on thestand or on the 14-function footcontrol panel.

Ageing of the lamp reducesthe amount of light.

u Switch halogen lamps. [} 192]

u Change the Superlux Eye lightsource lamp module. [} 194]

Light guide not correctlyinserted on the microscope.


Defective light guide (illumi-nation not uniform).


The lamp reflector for thehalogen lamp is not sittingcorrectly in the lamp bulb.

u Press the lamp reflector into thelamp bulb. [} 192]

The LED light source isdefective, and the lightintensity is 50%.


Illumination in the surgical field istoo bright.

Brightness level set too high. u Decrease the brightness on thestand or on the 14-function footcontrol panel.

u Switch off the light source onthe stand. Illuminate the OPfield with an OP lamp.


Defective light control. u Activate manual mode. [} 190]

Red reflex is too dark or non-existent.

Red reflex illumination is notactivated.

u Switch the red reflex illumi-nation on. [} 156]

Soiled objective lens. u Clean the objective lens.

Light guide not correctlyinserted on the microscope.


Light guide is damaged. u Contact ZEISS Service.

The lamp reflector for thehalogen lamp is not sittingcorrectly in the lamp bulb.

u Press the lamp reflector into thelamp bulb. [} 192]

The surgical microscope is notoriented.

u Place the device in the workingposition. [} 120] The mainmicroscope axis must coincidewith the optical axis of thepatient’s eye.


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Fault Cause Remedy

Image on video monitor is too dark,or there is a high level of noise.

Insufficient light. u Increase the brightness level ofthe illumination.

Incorrect light meteringmethod selected for theintegrated camera.

u Activate the "Integral" lightmetering method. [} 162]

For external cameras u Remove the fixed stop from theexternal camera adapter.

The surgical microscope's motorizedfocus or zoom functions are inoper-ative.

Stand electronics failure. u Operate the device in manualmode. [} 191] Use the manualzoom on the surgicalmicroscope.

Motion of suspension arm too stiff. Friction adjustment knobtightened too firmly.

u Rotate the [Weight balancing]rotary knob until the suspensionarm becomes mobile. [} 111]

The surgery profile cannot bechanged via the configured buttonon the handgrip.

You are not in the main menu. u Return to the main menu.

No video image. Connection cable not properlyconnected.

u Check all connections.

Stand wobbles. Floor not level. Stand base notappropriately positioned.

u Reposition the stand base.[} 118]

10.3.2 Integrated HD video and image recording faults

Fault Cause Remedy

Data cannot be saved. USB storage device isdefective.

u Check to make sure the USBstorage device is working.

u If the USB storage device is notworking properly, replace it.

USB storage format is notsupported.

u Use USB storage devices withFAT32 or NTFS.

No storage capacity. u Delete data you no longer need.Note the available storage spacedisplay.

No network connection. u Establish a network connection.[} 145]

No network authorization. u Check to make sure the networkand directories are beingshared.

u Adjust the read and writepermissions.

10 Troubleshooting Instructions for UseOPMI LUMERA 70010.3 Faults (without messages)

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Fault Cause Remedy

Data cannot be displayed or playedback.

Non-supported file formatimported or saved to the LAN.

u Use supported file formats.

Video with incorrect videosystem was imported or savedto the LAN.

u Set the device to the videosystem for your country (PAL orNTSC).

u Restart the device.

USB storage device wasremoved and reinserted in themeantime. When the USBstorage device is removed, thedevice automatically creates anew, empty patient file.

u Select the desired patient file.[} 165]

Integrated video and imagerecording not functioning.

USB storage device wasremoved and reinsertedrepeatedly during recording.

u Restart the device after surgery.

Selected patient cannot be deleted. Patient is current patient. u Select another patient. [} 165]

u Delete the desired patient.

10.3.3 14-function foot control panel faults

Fault Cause Remedy

The 14-function foot control panel isnot functioning.

The batteries are dead. u Replace the batteries.

The rechargeable batteries aredead.

u Replace the rechargeablebatteries.

Failure of individual buttonfunctions.

u Reconfigure the buttonfunctions. This can only be doneif the buttons on the device areconfigurable.

Radio link failure/fault. u Establish a cable connection.[} 198]

The 14-function foot controlpanel's position sensor alwaysdetects the rest position.

u Establish a cable connection.[} 198]

Weak radio signal. u Establish a cable connection.[} 198]

No pairing with stand. u Perform pairing. [} 140]

The surgery profile cannot bechanged via the configured buttonon the 14-function foot controlpanel.



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Fault Cause Remedy

Functions are being triggeredunintentionally.

A button on the 14-functionfoot control panel has becomemechanically stuck after beingpressed.

u Place the 14-function footcontrol panel in its rest position.


The 14-function foot controlpanel is sending an erroneousactivation signal.

u Place the 14-function footcontrol panel in its rest position.


The wrong 14-function footcontrol panel is being used.

u Check the marking. The markingon the stand and the indicatoron the 14-function foot controlpanel must match.

u Perform pairing. [} 140]

10.3.4 Wired 14-function foot control panel faults

Fault Cause Remedy

The 14-function foot control panel isnot functioning.

The 14-function foot controlpanel is not plugged in.

u Check to make sure the 14-function foot control panel isproperly plugged in on thestand.

Intermittent loss of functionality. Failure of individual buttonfunctions.


The surgery profile cannot bechanged via the configured buttonon the 14-function foot controlpanel.


10 Troubleshooting Instructions for UseOPMI LUMERA 70010.4 Troubleshooting work

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10.4 Troubleshooting work

10.4.1 Activating manual mode

1

Figure 77: Activating manual mode

1 [Manual mode] switch

CAUTION! Risk of injury caused by malfunctioning motor electronics!

In the case of malfunctioning motor electronics, the device maymake uncontrollable movements or main functions such as XYmovement, focus, zoom and light control may become impaired.



Action 1. Press the [Manual mode] switch.

ð The light sources are at medium intensity

ð The XY coupling, focus and zoom motor are inactive

ð The filters are the in swiveled-out position. For filters thatwere previously in the swiveled-in position: note the"Maximum radiation exposure times" table. [} 27]

ð The control panel is black

ð The shutters are in the swiveled-out position

2. If manual mode is activated: operate the device manually.[} 191]

Instructions for Use 10 TroubleshootingOPMI LUMERA 700 10.4 Troubleshooting work

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10.4.2 Operating the device in manual mode

1 2 3

Figure 78: Operating the device in manual mode

1 Zoom adjustment knob 2 [SCI illumination] rotary knob

3 [Integrated slit illumination] rotary knob

Prerequisite þ Manual mode is activated.

Action 1. Position the surgical microscope. Move the suspension arm inthe desired direction.

2. Focus the surgical microscope. To do this, move the suspensionarm up and down.

3. Set the magnification on the manual zoom adjustment knob.

4. Set the SCI illumination. To do this, rotate the [SCI illumination]rotary knob to the following positions:

ð Left position: light emitted generates a red reflex.

ð Right position: light emitted illuminates the entire field ofview

5. Set the integrated slit illumination. To do this, rotate the[Integrated slit illumination] rotary knob to the followingpositions:

ð Left position: slit illuminator from the left

ð Center position: standard OPMI illumination

ð Right position: slit illuminator from the right

Tip: In manual mode, you can switch off the light sources for lightguides which you no longer need. To do this, press the [Open lampmodule] button on the lamp housing.


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10.4.3 Changing the halogen lamp

1

2

4 5

3

Figure 79: Changing the halogen lamp

1 [Open lamp module] button 2 Lamp module

3 Lamp reflector of thehalogen lamp

4 Lamp bulb of the halogenlamp

5 Ceramic base of the lamp module

CAUTION! Risk of burn injury caused by a defective halogen lamp!

Damage to new halogen lamp caused by body oils.

u Wait several minutes until the halogen lamp is cool.

u Replace the halogen lamp with heat-reflective protectivegloves.

Material • Halogen lamp: 12 V, 100 W


Action 1. Press the [Open lamp module] button.

ð The lamp module will eject partially.

2. Pull out the lamp module.

3. CAUTION! Risk of burns due to hot halogen lamp! Removethe defective halogen lamp from the spring-loaded mount.

4. Pull the ceramic base from the contact pins of the halogenlamp.

5. NOTE! New halogen lamp can be damaged by contact!Plug the ceramic base onto the contact pins of the newhalogen lamp.

6. Insert new halogen lamp.

7. Press the halogen lamp into the spring-loaded mount.

8. Push the lamp module, including the new halogen lamp, backinto the device.

9. Turn on the device at the power switch.

10. Check both halogen lamps for functionality.


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10.4.4 Swiveling the backup xenon lamp into position andresetting the remaining service hours

2

4

3

1

Figure 80: Swiveling the backup xenon lamp into position

1 Lamp housing 2 Lamp module

3 [Backup xenon lamp] switch 4 [Open lamp module] button

CAUTION! Risk of injury caused by lamp rupture!

Lamp rupture may lead to jamming of the lamp module and failureof the electronics modules.

u The lamp module may be changed only by appropriatelytrained personnel.

u Before opening the lamp housing: move the device to aposition in which falling particles cannot put the patient or userat risk.

u If the lamp module is blocked or illumination is no longeroperable, the device may not be used any longer. Contact ZEISSService.




2. Pull out the lamp module as far as it will go.

3. Swivel the second xenon lamp (backup) into position. To dothis, rotate the [Backup xenon lamp] switch clockwise 180°until it snaps into place.

ð The red segment in the [Backup xenon lamp] switch willappear.

4. Push the lamp module all the way back into the lamp housing.


ð The red segment in the [Backup xenon lamp] switch willilluminate.


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ð The following message will appear on the control panel:"OPMI light source: spare lamp is in use, please changemain lamp."

6. Acknowledge the error message.

7. Reset the remaining service hours counter to its initial value of500. To do this, go to [System Settings] > [Tab 2] > [Lampservice life] > [Reset] from the main menu.

ð The following prompt will appear: "Do you want to resetthe service hours of the lamps?"

8. To reset the service hours: tap the [Yes] button.

ð The remaining service hours will be reset to 500

Tip: To be safe, keep a backup lamp module with two new xenonlamps at hand.

10.4.5 Changing the Superlux Eye light source lamp module

3

5

12

4

Figure 81: Changing the Superlux Eye light source lamp module

1 Bolt 2 Original transport packaging

3 Lamp module 4 Borehole

5 [Open lamp module] button


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CAUTION! Risk of injury caused by lamp rupture!

Lamp rupture may lead to jamming of the lamp module and failureof the electronics modules.

u The lamp module may be changed only by appropriatelytrained personnel.

u Before opening the lamp housing: move the device to aposition in which falling particles cannot put the patient or userat risk.

u If the lamp module is blocked or illumination is no longeroperable, the device may not be used any longer. Contact ZEISSService.

Material • Xenon backup lamp module with 2 xenonlamps for Superlux Eye




2. Slide the original transport case over the module until the boltsnaps into the borehole. This unlocks the stop.

3. NOTE! Using the correct lamp module. Use only thebackup lamp module prescribed above. Remove the oldlamp module and insert the backup module.


5. Check the function of the xenon lamp and backup xenon lamp.

6. Reset the remaining service hours counter to its initial value of500.

7. Package the old lamp module in the backup lamp module'soriginal transport packaging.

8. Fill in the enclosed return card and send the old lamp moduleto ZEISS Service.

Use only the original transport packaging! It features explosionprotection for potentially defective xenon lamps.

10.4.6 Setting the gas spring on the integrated 22" monitorIf the integrated 22" monitor is lowering on its own, the gas springon the suspension arm can be readjusted.

Tools • M5 hex key

Action 1. Align the suspension arm and the support arm horizontally.

2. Tighten the hexagon socket screw on the gas spring clockwise(+) until the integrated 22" monitor remains in the desiredposition.


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If the suspension arm continues to lower on its own, the gas springis defective.

3. Inform ZEISS Service!

10.4.7 Increasing mobility of the suspension arm on theintegrated 22" monitorIf the 22" monitor is making undesired swivel movements to theleft or right, the mobility of the suspension arm can be increased.

Tools • M2.5 hex key

• M5 hex key

Action 1. Loosen the securing screw on the support arm. To do this, turnthe securing screw counter clockwise using an M2.5 hex key.

2. Remove the plastic cover on the suspension arm.

3. Tighten the adjustment screw on the suspension arm until thedesired level of mobility is achieved. To do this, turn theadjustment screw clockwise using an M5 hex key.

4. Retighten the securing screw on the suspension arm. To dothis, turn the securing screw clockwise using an M2.5 hex key.


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5. Reattach the plastic cover.

10.4.8 Increasing mobility of the monitor mount on theintegrated 22" monitorIf the 22" monitor is making undesired tilting movements, themobility of the monitor mount can be increased.


Action 1. Tighten the hexagon socket screw on the monitor mountclockwise until the integrated 22" monitor remains in thedesired position.

10.4.9 Increasing mobility of the monitor mount on theintegrated CALLISTO eye Panel PC support armIf the CALLISTO eye Panel PC is making undesired tiltingmovements, the mobility of the monitor mount can be increased.


Action 1. Tighten the hexagon socket screw clockwise until theintegrated CALLISTO eye Panel PC remains in the desiredposition.


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10.4.10 Establishing cable connections for the 14-function footcontrol panelIf the 14-function foot control panel continues to be non-opera-tional after pairing, connect it to the device using a cable.

Material • 3m, 6m or 10m cable


Action 1. Insert the 6-pin connector into the socket on the 14-functionfoot control panel.

2. Insert the 4-pin connector (straight or angled) into the socketon the stand.

10.4.11 Displaying the firmware versionsAn overview of the installed firmware versions is available in the"Versions" menu. The information displayed varies depending onthe equipment the device is outfitted with.



3. Tap the [Versions] button.

ð The "Versions" menu will appear.

4. To view all firmware versions: tap the arrow buttons.

ð The menu will scroll up or down.

10.4.12 Opening the service menuThe service menu is password-protected and may only be accessedby personnel trained by ZEISS.

Prerequisite þ The service PIN is available



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3. Tap the [Service PIN] submenu button.

ð The "Service PIN" menu will appear.

4. To open the service menu: enter the service PIN.

Instructions for Use 11 Technical specificationsOPMI LUMERA 700 11.1 Essential performance features

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11 Technical specifications

11.1 Essential performance featuresThe device does not have any essential performance features asdefined in IEC 60601-1.

11.2 Compliance

Guidelines with which the device complies

• OPMI LUMERA 700 complies with Medical Device Directive93/42/EEC: Class I

It is labeled with

• This device satisfies the US American and Canadian safetyregulations for medical electrical devices/systems.

It is labeled with

• The device complies with Directive 2011/65/EU on therestriction of the use of certain hazardous substances inelectrical and electronic equipment.

Classification of the device according to IEC 60601-1

The device is classified as follows:

• Degree of protection against electric shock: Class I

• Degree of protection against entry of water: IP 20

• Electromagnetic compatibility (EMV): Fulfills IEC 60601-1-2,Class B (as per CISPR 11)

• Operating mode: continuous operation

Classification of the 14-function foot control panel

• See also document G-30-2021 (Radio Approval Information).The radio frequency approvals apply only to the wireless versionof the 14-function foot control panel.

11 Technical specifications Instructions for UseOPMI LUMERA 70011.3 Electrical data

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11.3 Electrical data

11.3.1 Stand

Values

Rated voltage (115): 100 - 125 V AC

(230): 220 - 240 V AC

Total current consumption at 115 V 1200 VA maximum

Total current consumption at 230 V 1200 VA maximum

Rated frequency 50 - 60 Hz

Degree of protection (EN 60529) IP20

Protection class (EN 60601-1) I

Fuses Automatic fuse

Electrical output 100/240 V AC

500 VA maximum

Remote connection 24 V

0.5 A

Network connection RJ45

11.3.2 Light sources

Unit Superlux Eye Halogen LED

Illumination type Fiber optics Fiber optics Fiber optics

Main lamp Xenon short-arcreflector bulb

Halogen lamp LED

Backup lamp Xenon short-arcreflector bulb

Halogen lamp -

Color temperature K 5000 (±500) 3200 (±500) 5500 (±500)

Voltage V - 12 -

Rated output W 180 100 50

Lamp change Manual Automatic Automatic

Retina protectionfilter

Standard Standard Standard

Fluorescence filter485 nm

Optional Optional Optional

HaMode filter Standard - Standard

Gray filter 25% - - Optional

Instructions for Use 11 Technical specificationsOPMI LUMERA 700 11.3 Electrical data

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11.3.3 Integrated HD camera

Unit HD ready Full HD Full HD with videorecording andstreaming

1-Chip HD cameraimage sensor

1/3" progressive HD MOS sensor

3-Chip HD cameraimage sensor

Three 1/3" progressive HD MOS sensors

Resolution Pixels 1280 x 720 1920 x 1080 1920 x 1080

Signal-to-noise ratio dB 54

Scanning systemPAL

Hz Progressive: 50 full frames/second

Scanning systemNTSC

Hz Progressive: 59.94 full frames/second

11.3.3.1 Digital video outputs


HD-SDI (-0.8 Vp-p/75 ΩPAL) Pixels / Hz (PAL) 720p / 50 720p / 50

1080p / 50

720p / 50

1080p / 50

Pixels / Hz (NTSC) 720p / 59.94 720p / 59.94

1080p / 59.94

720p / 59.94

1080p / 59.94

DVI (according to DVI

Standards)

Pixels / Hz (PAL) 720p / 50 720p / 50

1080p / 50

720p / 50

1080p / 50

Pixels / Hz (NTSC) 720p / 59.94 720p / 59.94

1080p / 59.94

720p / 59.94

1080p / 59.94

11.3.3.2 Analog video output ports


Composite (-1.0 Vp-p/75

ΩPAL composite)

Pixels / Hz (PAL) 567i - -

Pixels / Hz (NTSC) 480i / 59.94 - -

Y/C (-1.0 Vp-p/75 Ω luminance)

(-0.3 Vp-p/75 Ω chroma)

Pixels / Hz (PAL) - 576i / 50 576i / 50

Pixels / Hz (NTSC) - 480i / 59.94 480i / 59.94

11 Technical specifications Instructions for UseOPMI LUMERA 70011.3 Electrical data

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YPbPr (-1.0 Vp-p/75 Ω (Y))

(-0.3 Vp-p/75 Ω (Pb, Pr)

Pixels / Hz (PAL) 720p / 50 720p / 50

1080p / 50

720p / 50

1080p / 50

Pixels / Hz (NTSC) 720p / 59.94 720p / 59.94

1080p / 59.94

720p / 59.94

1080p / 59.94

11.3.4 Integrated HD video and image recording


Video resolution Pixels - - 1920 x 1080

Required storagespace

• Low

• Medium

• High

GB - -

• 1.8 GB per hour

• 3.2 GB per hour

• 4.6 GB per hour

Image frequency Hz - - 25/30 frames persecond (PAL/NTSC)

Video codec - - H.264

Video format mpg - - MPEG

Photo Format - - JPEG and TIFF(uncompressed)

Image resolution Pixels - - 1920x1080 (2.1megapixels)

Media for saving videos to USB

Storage device - - USB stick or HDD

Interface - - USB 2.0 (or higher)

File system - - FAT16, FAT32 orNTFS

Speed (read andwrite)

MB/s - - > 5

Media for saving videos to an IT network

Interface MBit/s - - ≥ 100

Protocol - - CIFS

Speed (read andwrite)

MB/s - - > 5

Instructions for Use 11 Technical specificationsOPMI LUMERA 700 11.4 Mechanical data

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11.3.5 Integrated keratoscope ring

Value

Wavelength 610 nm (±15 nm)

Radiation output 0.149 mW

Divergence of beam (opening angle) 100°

11.3.6 Integrated 22" monitor

Value

Input voltage 12 V DC (± 10%)

Current consumption < 5 A DC

Resolution 1680 x 1050 pixels

Reaction time 8 ms

Brightness 220 cd/cm2

Contrast 1600:1

Color display 16.7 m

Analog video inputs VGA, Y/C, composite

Digital video inputs DVI-D, DVI-A

COM port RS-232

11.4 Mechanical data

11.4.1 Integrated slit illumination

Value

Slit width • 0.2 mm

• 2 mm

• 3 mm

• 4 mm

Slit height 12 mm

Angle of illumination +6° or -6°

11.4.2 Integrated 22" monitor

Value

Weight 8 kg (±10 %)

Dimensions (W x H x D) 360 x 568 x 153 mm

11 Technical specifications Instructions for UseOPMI LUMERA 70011.5 Optical data

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Value

Screen diagonal 22"

11.5 Optical data

11.5.1 Surgical microscope

Value

Magnification (with objective lens f=200and eyepiece 10x)

3.5x - 21x

Magnification factor 0.4x - 2.4x

Zoom system Motorized

Focus Motorized

Total focus range 70 mm

Upward focus range 40 mm

Downward focus range 30 mm

11.5.2 Objective lenses

Unit f=175 f=200

Focal length mm 175 200

11.5.3 Objective lenses with support ring

Unit f=175 f=200 f=225

Focal length mm 175 200 225

11.5.4 Eyepieces

Unit 10x 12.5x

Magnification x 10 12.5

Focal length mm 25 20

Field of Vision mm 21 18

Distance of the exit pupil from the lastlens

mm 24 - 25.5 22 - 23.5

Diopter adjustment range dpt. +5 / -8 +5 / -8

Weight kg 0.120 0.115

Instructions for Use 11 Technical specificationsOPMI LUMERA 700 11.6 Dimensions and weights

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11.6 Dimensions and weights

11.6.1 Dimensions and swiveling ranges

AC

BD

E

FG

H

II

J

Figure 82: Dimensions and swiveling ranges

Item Value

Extension arm swiveling angle A 320°

Extension arm length B 450 mm

Suspension arm swiveling angle C 320°

Suspension arm length D 850 mm

XY coupling angle of rotation E 270°

Suspension arm stroke F ±360 mm

XY coupling travel range G 61 mm

Microscope tilt mechanism tilt angle H +90° / -20°

Foot dimension I 805 mm

Stand height J 1880 mm

11 Technical specifications Instructions for UseOPMI LUMERA 70011.6 Dimensions and weights

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11.6.2 Support arm for integrated CALLISTO eye Panel PCA

BC

D

E

F

G

H

I

J


Item Value

Monitor mount swiveling angle A 220°

Monitor mount length B 101 mm

C 70 mm

Support arm tilt angle D 45°

Extension arm swiveling angle E 210°

Support arm tilt angle F 45°

G 45 mm

H 70 mm

Extension arm length I 252 mm

VESA 75/100 interface tilt angle J 24°

Instructions for Use 11 Technical specificationsOPMI LUMERA 700 11.6 Dimensions and weights

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11.6.3 Support arm for integrated 22" monitor

J

A

B

C

D

E

F

G

H

I


Item Value

Monitor mount swiveling angle A 180°

Monitor mount length B 84 mm

Suspension arm tilt angle C ±41°

Suspension arm swiveling angle D 360°

Suspension arm tilt angle E ±41°

Extension arm swiveling angle F ±90°

G 180 mm

H max 380 mm

VESA 75/100 interface tilt angle I ±85°

VESA 75/100 interface angle of rotation J ±90°

11 Technical specifications Instructions for UseOPMI LUMERA 70011.6 Dimensions and weights

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11.6.4 Maximum weight capacity

A B

C

D

Figure 85: Maximum weight capacity

Item Value

Support arm for integrated 22" monitor A 10kg.

Support arm for integrated CALLISTO eyePanel PC

B 15 kg

Suspension arm (with mounted surgicalmicroscope [no tube, eyepieces, objectivelens] and XY coupling)

C 9 kg

Instrument tray D 13 kg

11.6.5 Total weight

Value

• Total weight with CALLISTO eye PanelPC and accessories

approx. 280 kg

Instructions for Use 11 Technical specificationsOPMI LUMERA 700 11.7 Ambient requirements for operation

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11.7 Ambient requirements for operationAll stand variants

Temperature +10 °C ... +40 °C

Rel. humidity 30% ... 75%

Air pressure 800 hPa ... 1060 hPa

11.8 Ambient requirements for transport andstorage

All stand variants

Temperature -25 °C ... +60 °C

Rel. humidity (without condensation)

10% ... 90%

Air pressure 500 hPa ... 1060 hPa

11.9 Guidance and manufacturer´s declaration –electromagnetic immunityThe device is subject to specific precautions with regard to electro-magnetic compatibility (EMC) in the area of Professional HealthcareFacility Environment. In order to avoid the occurrence of EMCdisturbances, the device may only be installed, started up andmaintained in the manner indicated in these Instructions for Useand only with components supplied by ZEISS.

WARNING! Malfunction caused by other devices!

Do not install or operate the OPMI LUMERA 700 in direct proximityto other devices (with the exception of the combination of thedevices described in these Instructions for Use) as this can impairthe function of the device.

u If it cannot be avoided that the OPMI LUMERA 700 is operatedin proximity to other devices, the proper function of theOPMI LUMERA 700 must be monitored.

WARNING! Malfunction caused by non-approved components!

Electrical devices can influence each other as a result of theirelectromagnetic radiation. The use of non-approved componentscan cause increased emissions or reduce the device's immunity.

u Only use accessories, transformers, cables and spare partswhich are specified in these Instructions for Use or which havebeen approved by ZEISS for this device.

11 Technical specifications Instructions for UseOPMI LUMERA 70011.9 Guidance and manufacturer´s declaration – electromagnetic immunity

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WARNING! Loss of performance caused by HF units!

u Do not use any portable or mobile HF communicationequipment or transmitters (including peripheral devices such asantenna cables or external antennas) in the proximity of theOPMI LUMERA 700 (minimum distance 30 cm). It cannot beruled out that the function of the device will be impaired orthat the performance of the device will deteriorate.

u Do not use cell phones near the OPMI LUMERA 700. Theyrepresent a potential risk for the proper functioning of medicalequipment. Malfunctions may occur, depending on a variety oflocal factors. They cannot be predicted and can by no meansbe estimated.

u Please follow the EMC guidelines on the following pages.

NOTE Disturbances caused by electromagnetic radiation!

The OPMI LUMERA 700 may experience interference from otherdevices even if the other devices comply with the emission require-ments applicable to them as per CISPR.

u Do not use the OPMI LUMERA 700 when it is located next to,or stacked on top of, other devices.

u If it is necessary to operate the device next to, or stacked ontop of, other devices, monitor the OPMI LUMERA 700 toensure its normal operation in the arrangement in which it isused.

u If you use the OPMI LUMERA 700 together with other devicesthat generate high-frequency waves or high voltages, check theeffects that these devices have before using them, and installthe device in such a way so as to minimize disturbances causedby high-frequency waves.

The following device functions have been defined for the immunitytest:

• The CALLISTO eye user interface is accessible at all times.

• The integrated HD camera's video signal is accessible at alltimes.

• Magnification of the surgical field is accessible at all times.

• Illumination of the surgical field is accessible at all times.

• Focusing on the surgical field is accessible at all times.

Instructions for Use 11 Technical specificationsOPMI LUMERA 700 11.9 Guidance and manufacturer´s declaration – electromagnetic immunity

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11.9.1 EMC - electromagnetic compatibility IEC 60601-1-2

11.9.1.1 Electromagnetic disturbance emissions

The OPMI LUMERA 700 is intended for operation in an electromagnetic environment as specified below. Thecustomer or the user of the OPMI LUMERA 700 is responsible for ensuring that the device is operated in suchan environment.

Interference measurements Compliance

HF emissions as per CISPR 11 Group 1

HF emissions as per CISPR 11 Class B*

Harmonic emissions as per IEC61000-3-2

Class A*

Emission of voltage fluctuations/flicker as per IEC 61000-3-3

Compliant*

Note*

* The OPMI LUMERA 700 as a system combination with CALLISTO eye Panel PC (model I with SN 690912xxxand 690914xxx) is suitable for use in facilities other than locations in residential environments and thosedirectly connected to the public power supply network which also supplies buildings used for residentialpurposes, provided that the following warning note is observed:

WARNING: This system is only intended for use by trained medical personnel. This is a class A system asspecified in CISPR 11. In residential areas, this device may cause radio interferences necessitating appropriatecorrective measures to be taken, such as reorientation, repositioning or shielding of the OPMI LUMERA 700,or filtering of the connection to the site of use.

11.9.1.2 Electromagnetic immunity for all ME equipment and MEsystems


Electromagnetic immunity tests IEC 60601 test level Compliance level

Electrostatic discharge (ESD) as perIEC 61000-4-2

± 8 kV contact discharge

± 8 kV contact discharge

±15 kVair discharge

±15 kVair discharge

Electrical fast transient/burstimmunity as per IEC 61000-4-4

± 2 kV for power supply lines

± 2 kV for power supply lines

±1 kV for input/output lines

±1 kV for input/output lines

Surges as per IEC 61000-4-5 ± 1 kV phase-to-neutral voltage

± 1 kV phase-to-neutral voltage

± 2 kV phase/neutral to ground voltage

± 2 kV phase/neutral to ground voltage

11 Technical specifications Instructions for UseOPMI LUMERA 70011.9 Guidance and manufacturer´s declaration – electromagnetic immunity

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Magnetic field for supplyfrequency (50/60 Hz) as per IEC61000-4-8

30 A/m 30 A/m

Voltage dips, short interruptionsand voltage variations as per IEC61000-4-11

0% UT for 1/2 cycle 0% UT for 1/2 cycle

0% UT for 1 cycle 0% UT for 1 cycle

70% UT for 25/30 cycles 70% UT for 25/30 cycles

0% UT for 250/300 cycles 0% UT for 250/300 cycles

11.9.1.3 Electromagnetic immunity for non-life-supporting MEequipment and ME systems


Electromagnetic immunity tests IEC 60601 test level Compliance level

Conducted HF disturbances as perIEC 61000-4-6

3 V150 kHz to 80 MHz

3 V

6 VISM and amateur radio bandsbetween 150 kHz and 80 MHz

6 V

Radiated HF disturbances as perIEC 61000-4-3

10 V/m 80 MHz to 2.7 GHz

10 V/m

Radiated HF disturbances fromnear fields of wireless communi-cation devices as per EN61000-4-3

27 V/m

385 MHz

27 V/m

28 V/m

450 MHz, 810 MHz – 2.45 GHz

28 V/m

9 V/m

710 MHz – 780 MHz, 5.24 GHz – 5.785 GHz

9 V/m

Instructions for Use 12 Accessories and spare partsOPMI LUMERA 700 12.1 Accessories

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12 Accessories and spare parts

12.1 AccessoriesThese Instructions for Use describe accessories that are notessential components of the individual deliveries. A current list ofaccessories can be obtained from your ZEISS contact partner.


Use only accessories and spare parts which are approved by ZEISSfor this device. When using accessories and spare parts that are notapproved by ZEISS, safe operation of the device cannot beguaranteed.

12.1.1 Video accessoriesFor external video accessories for this surgical microscope, pleaserefer to the separate product overview G-30-1888.

12.1.2 14-function foot control panel

Designation Specification Order no.

FCP WL Wireless 304970-9020-000

FCP Wired 304970-9015-000

Cable 3 m 304970-8730-000

Cable 6 m 304970-8760-000

Cable 10 m 304970-8710-000

12.1.3 Fundus viewing systems


RESIGHT 500 Motorized focusing unit 302721-9030-000

RESIGHT 700 Manual focusing unit 302721-9020-000

For additional components, please refer to the RESIGHT 500 & RESIGHT 700 Instructions for Use

12.1.4 Additional illumination


VISULUX Motorized fiber slit illuminator 000000-1100-155

FC angular illumination - 303371-9004-000

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12.1.5 Sterilizable caps


6x sterilizable caps, 22 mm - 305810-9001-000

6x sterilizable caps(OPMI LUMERA 700)

- 305810-9017-000

6x steril. caps, 49 mm (180°tiltable tube)

- 305810-9003-000

6x sterilizable caps, 12 mm - 305810-9002-000

2x handgrips, 6x 22mm sterilizablecaps

- 305810-9015-000

2x sterilizable caps (VISULUX) - 305810-9009-000

12.1.6 Drapes


OPMI drapes, sterile (5 pcs.) 1220 mm x 2090 mm 306070-0000-000

OPMI drapes, sterile (5 pcs.) 1220 mm x 3000 mm 306071-0000-000

Drapes (10 pcs.) 460 mm x 330 mm 306084-0000-000

Drapes for CALLISTO eye (80 pcs.) - 301640-0014-100

12.2 Spare parts

12.2.1 Lamps and light guides


Halogen lamp (2 pcs) 12 V, 100 W 380079-9040-000

Backup lamp module for SuperluxEye with 2 xenon lamps

- 304977-9038-000

S light guide 2.0 m 303481-9020-000

S light guide 2.5 m 303481-9025-000

12.2.2 Dust cover


Dust cover, blue, with ZEISS logo - 000000-1055-278

12.2.3 Network cable


Network cable 2x RJ45, 10 m 305946-8660-000

Instructions for Use 12 Accessories and spare partsOPMI LUMERA 700 12.3 Components

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Patch cable - 000000-2142-522

12.2.4 Country-specific power cable


Europe - 000000-0301-997

UK - 000000-0400-264

Switzerland - 309850-9011-000

Argentina - 000000-0434-527

Brazil - 000000-0527-730

China - 000000-0475-507

12.3 Components

12.3.1 Tubes for surgical and assistant's microscopes


Invertertube E Motorized 303797-9140-000

Invertertube Manual 303797-9120-000

45° inclined tube - 303784-0000-000

180° tiltable tube - 303791-0000-000

12.3.2 Eyepieces for surgical and assistant's microscopes


Eyepiece (2 pcs.) 10x 305542-0000-000

Eyepiece (2 pcs.) 12.5x asph. 305543-9901-000

Eyepiece with reticle (for mainoperator only)

10x 000000-1023-184

Eyepiece with reticle (for mainoperator only)

12.5x asph. 000000-1023-188

12.3.3 Intermediate pieces for surgical microscope


Intermediate piece 11 mm 303032-9002-000

Rotary dovetail for binocular tubes - 301007-0000-000

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12.3.4 Objective lenses


Objective lens f = 200 mm 302652-9905-000

Objective lens f = 175 mm 302651-9905-000

Objective lenses with support ring f = 175 mm 302671-9905-000



12.3.5 Coobservation


Stereo coobservation module - 000000-1063-869

8° assistant's microscope withmagnification changer

- 302624-9901-000

0° assistant's microscope withmagnification changer

- 302952-0000-000

12.3.6 Integrated components (factory installed)


SCI illumination - 302681-9023-000

SCI illumination system withintegrated slit illuminator

- 302681-9024-000

Superlux Eye light source - 304977-9023-000

LED light source - 304977-9055-000

Halogen light source - 304977-9052-000

Dual light source, LED + LED • LED

• LED

• S light guide

304977-9055-000

304977-9055-000

303481-9025-000

Dual light source, LED + SuperluxEye

• LED

• Superlux Eye

• S light guide

304977-9055-000

304977-9023-000

303481-9025-000

Dual light source, LED + halogen • LED

• Halogen

• S light guide

304977-9055-000

304977-9052-000

303481-9025-000

Dual light source, Superlux Eye +halogen

- 304977-9024-000

Instructions for Use 12 Accessories and spare partsOPMI LUMERA 700 12.4 UC kits

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Gray filter (25%) for LED lightsource

- 000000-1124-845

Assistant's microscope withelectrical zoom system

- 302681-9100-000

Assistant's microscope withmanual 5x magnification changer

- 302681-9110-000

Integrated keratoscope ring - 302681-9160-000

IDIS - 302681-9158-000

Overhead display - 305953-9082-000

Instrument tray - 00000-1352-729

12.3.7 CALLISTO eye


CALLISTO eye BASIC V3.5 With CALLISTO eye Panel PC (model I) 301640-3000-350

CALLISTO eye ASSISTANCE V3.5 With CALLISTO eye Panel PC (model I) 301640-3010-350

CALLISTO eye ASSISTANCEmarkerless V3.5

With CALLISTO eye Panel PC (model I) 301640-3020-350

CALLISTO eye BASIC V3.6 With CALLISTO eye Panel PC (model I) 301640-3000-360

With CALLISTO eye Panel PC (model II) 301640-4000-360

CALLISTO eye ASSISTANCEmarkerless V3.6

With CALLISTO eye Panel PC (model I) 301640-3020-360

With CALLISTO eye Panel PC (model II) 301640-4020-360

IOLMaster 500, reference imageoption

- 000000-1865-713

Support arm For CALLISTO eye Panel PC 301640-9020-000

Cart For CALLISTO eye Panel PC 301640-9200-200

Table stand For CALLISTO eye Panel PC 301640-9000-200

System cable set together withtrolley or table stand

• Set of cables

• Network cable

• 10 m

• 10 m

302755-8640-000

302755-8641-000

12.4 UC kitsThe following UC kits (upgrade components) are integrated eitherin or on the device and must be installed by ZEISS Service afteracquisition.

12 Accessories and spare parts Instructions for UseOPMI LUMERA 70012.4 UC kits

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UC kit, Superlux Eye light source Retrofit of a Superlux Eye light source forhalogen/Superlux Eye or LED/Superlux Eye duallight source.

304977-9027-500

UC kit, halogen light source Retrofit of a halogen light source for SuperluxEye/halogen or LED/halogen dual light source.

304977-9025-500

UC kit, LED light source Retrofit of an LED light source for LED/LED,Superlux Eye/LED or halogen/LED dual lightsource.

304977-9055-500

UC kit, LED light source Changeover to simple LED light source forSuperlux Eye or halogen

304977-9055-500

UC kit, 485 nm fluorescenceexciter filter

For LED light source 304977-0016-500

UC kit, 485 nm fluorescenceexciter filter

For Superlux Eye light source 304977-0015-500

UC kit, integrated HD 3-chipcamera

- 302681-9740-500

UC kit, integrated HD recording - 302681-9765-600

UC kit, integrated 22" monitorwith support arm

- 305953-9037-500

UC kit, integrated 22" monitorwith support arm and instrumenttray

- 305953-9038-500

UC kit, overhead display - 305953-9082-500

UC kit, manual SCI illuminationbutton

- 302681-8456-500

UC kit, keratoscope ring - 302681-9160-500

UC kit, IDIS Can only be retrofitted in devices with serialnumbers 6634101596 or higher

302681-9158-500

UC kit, FCP to FCP WL - 304970-9021-500

UC Kit, ethernet - 305953-9081-500

UC kit, support arm For CALLISTO eye Panel PC 301640-9020-500

Instructions for Use 13 DecommissioningOPMI LUMERA 700 13.1 Cleaning before storage

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13 Decommissioning

13.1 Cleaning before storage

13.1.1 Cleaning the device and accessoriesAction u Clean the device and any accessories which are no longer

needed as described in "Cleaning and disinfection [} 177]".

Instructions for Use 14 Packaging and transportOPMI LUMERA 700 14.1 Preparing for transport

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14 Packaging and transport

14.1 Preparing for transport

14.1.1 Placing the device in the transport position

CAUTION! Risk of crushing caused by rotating support and suspensionarms!

Fingers may be crushed between the stand column and the supportarm as well as between the support arm and the suspension arm.

u Never touch this area while moving these parts.


Action 1. Remove the power plug from the power outlet.

2. Place the support arm and suspension arm in the followingtransport position.

3. For integrated CALLISTO eye Panel PC: place the support arm inthe following transport position and press the locking leverdown.

ð The integrated CALLISTO eye Panel PC is locked.

14 Packaging and transport Instructions for UseOPMI LUMERA 70014.1 Preparing for transport

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4. For integrated 22" monitor: place the integrated 22" monitor inthe following transport position.

5. Feed the supplied Velcro tape through the bracket on the 22"monitor and wrap it around the suspension arm and supportarm.

ð The integrated 22" monitor is locked.

6. Hang the 14-function foot control panel on the foot controlpanel bracket.

7. Coil the cable up.

8. Hang the cable on the cable holder.

Instructions for Use 15 DisposalOPMI LUMERA 700 15.1 Disposal of the device

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15 Disposal

15.1 Disposal of the deviceu Keep packing material in the event of a relocation or repair.

u If you want to dispose of the packing material: Dispose ofpacking material by sending it for recycling through anacknowledged collection system.

The device contains electronic components with integratedbatteries.

u Dispose of the device and integrated batteries correctly, inaccordance with national legislation.

The device specified on the delivery note must not be disposed ofvia household waste or communal disposal companies according tothe applicable EU guidelines valid at the time the device was placedon the market.

u For more information about the disposal of the device, pleasecontact the ZEISS contact partner in your country.


u If you want to sell the device or its components: Inform thepurchaser that they must dispose of the device according to theregulations valid at that time.

Instructions for Use GlossaryOPMI LUMERA 700

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Glossary

Automatic fuseAn overcurrent protection device whichswitches the system off in the event of ashort.

BNCBNC (Bayonet Neill Concelman) is a coaxialconnector with bayonet lugs for high-frequency applications.

CompositeIn composite video signals, color,brightness and synchronization informationare combined and transmitted via a singlecable.

Depth of fieldThe range of depth that appears sharplydefined through the microscope.

DHCPDHCP (Dynamic Host ConfigurationProtocol) is a network configuration fordynamically assigning IP addresses.

DINDIN (German standards association)

Diopter scaleElement of an eyepiece for reading off theset refraction value.

DrapesSterile covers for surgical microscopes.

DVIDVI (Digital Visual Interface) is an electronicinterface for the transfer of digital andanalog video content.

Electromagnetic compatibility (EMC)EMC (electromagnetic compatibility) desig-nates the usually desired state in whichtechnical devices do not impede each otherby undesired electric or electromagneticeffects (non-interference).

EyecupEyepiece control element used to shield theeyepiece against scattered light during eye-controlled focusing.

FCPThe FCP is a wired foot control panel.

HD-SDIHD-SDI (High Definition Serial DigitalInterface) is a connection used to transmituncompressed video signals.

HFHF (high frequency)

IDISIntegrated Data Injection System

IECInternational Electrotechnical Commission

Incision/LRIA CALLISTO eye assistance function forpositioning incisions and LRIs.

IOLIOL (intraocular lens) is an artificial lens inthe eye.

IPThe IP (Internet Protocol) is a communica-tions protocol to transfer data in theInternet or a network.

Glossary Instructions for UseOPMI LUMERA 700

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K TRACKA CALLISTO eye assistance function usedtogether with the keratoscope to visualizethe corneal curvature.

LANLAN (local area network)

LEDLED is a light emitting diode.

Manual modeUsed to switch from working mode tomanual mode in the event of a device fault.

NTSCNTCS (National Television SystemsCommittee) is a US American institutionwhich defined the first color transmissionsystem.

PairingPairing is the term used to describe thefixed relative assignment of the suspensionsystem and foot control panel.

PALPAL (Phase Alternating Line) is a color trans-mission system in analog TV systems.

RESIGHT 500A manual fundus viewing system for stereo-scopic imaging of the posterior segment ofthe eye.

RESIGHT 700An electric fundus viewing system forstereoscopic imaging of the posteriorsegment of the eye.

Retina protection filterFilters out the blue portion of the lightbeam and makes it possible to operate forlonger periods of time. This is also referredto as a blue barrier filter.

RHEXISA CALLISTO eye assistance function whichprovides assistance when reaching thedesired size and shape of the capsulorhexis.

SCISCI (Stereo Coaxial Illumination)

SIPSIP (Service Indentification Program)

UC kitUC (Upgrade Component) is a retrofit kit forZEISS devices or systems.

UDIUnique Device Identification (UDI)Standardized identification system formedical devices.

UDI Production Identifier (UDI-PI)Unique Device Identification - ProductionIdentifier

UDI-DIUnique Device Identification - DeviceIdentifier

USBUSB (universal serial bus) is a standardconnector to connect peripheral devices.

UVUV (ultraviolet)

WEEEWEEE (Waste of Electrical and ElectronicEquipment)

WLWL (Wireless)

WLANWireless Local Area Network

Instructions for Use GlossaryOPMI LUMERA 700

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Y/CAnother term for S-Video; color andbrightness signals are transmittedseparately.

YPbPrA color model that transmits brightnessinformation Y and color difference infor-mation Pb and Pr separately.

Z ALIGNA CALLISTO eye assistance function foraligning toric intraocular lenses.

Instructions for Use Keyword indexOPMI LUMERA 700

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Keyword index

Numerical14-function foot control panel

(see foot control panel) ........................... 432nd light source........................................... 815x magnification changer ...................... 42, 85

AAir humidity................................................. 20Ambient conditions

Operation ............................................. 211Transport .............................................. 211

Angle of illumination ................................... 25Anti-fogging agents................................... 177Assistant's microscope................................. 85

Control elements .................................... 55Device description................................... 42

Assistant's microscope focus knob............... 56Assistant's microscope locking button ......... 56Auto Delete Mode ....................................... 87

BBlue barrier filter.......................................... 24Blue value.................................................... 87

CCable deflector ............................................ 43Cable holder ................................................ 44Cable tray .................................................... 39CALLISTO eye

Ending control ...................................... 173Panel PC ................................................. 36Panel PC control elements................. 62, 63Transferring control .............................. 172

CE marking ................................................ 201Changing lamps

Halogen light source ............................. 192Superlux Eye light source ...................... 193

Chroma ....................................................... 87Cleaning

Mechanical surfaces.............................. 177Optical surfaces .................................... 177

Compliance ............................................... 201Composite video output .............................. 48Configuring optics ..................................... 139Connections

Assistant's microscope ............................ 47CALLISTO eye Panel PC (model I)............. 49

CALLISTO eye Panel PC (model II)............ 49Connector panel ..................................... 48Integrated HD camera............................. 48Surgical microscope ................................ 47

Control panel............................................... 61Bottom bar ............................................. 65Color code .............................................. 67Interactive buttons.................................. 67Keyboard ................................................ 70Navigation buttons ................................. 69Status bar ............................................... 66

Coobservation output .................................. 47Rotary knob ............................................ 55

CSA marking.............................................. 201

DDeepView.................................................... 83

Setting .................................................. 158Degree of protection ......................... 201, 202DHCP................................................. 143, 145Diopter scale................................................ 41Diopter setting ring...................................... 57Disinfection ............................................... 178Disposal

Batteries ............................................... 225Electronics ............................................ 225Packing material ................................... 225

DVI-D video output...................................... 48

EElectrical output......................................... 202Electrical safety ............................................ 18Electrical zoom system........................... 42, 85Electromagnetic compatibility .............. 19, 201EMC

Precautionary measures .......................... 19See electromagnetic compatibility........... 19

Environmental conditions ............................ 18Exposure

Automatic exposure.............................. 162Manual exposure .................................. 164

Exposure timeIntegrated slit illuminator ........................ 28Red reflex illumination ............................ 27Surrounding field illumination ................. 28

Eyecup................................................... 41, 57Eyepiece mount ........................................... 41

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FFast focus .................................................... 82

Configuration........................................ 150Fault signal

Halogen light source ............................... 51LED light source ...................................... 51Manual mode ......................................... 52Superlux Eye light source ........................ 50

FaultsExporting log files ................................. 183Foot control panel FCP.......................... 189Foot control panel FCP WL.................... 188Integrated HD video and image recording.... 187With messages...................................... 185Without message.................................. 187

Filter ............................................................ 38Firmware versions...................................... 198Fixing suspension arm position .................... 60Fluorescence filter 485 nm................... 38, 202Focus distance ........................................... 159Focus position ............................................. 53Foot control panel

Bracket ................................................... 44Buttons................................................... 58Configuration........................................ 147Joystick ................................................... 58Pairing .................................................. 140Rocker switches ...................................... 58

Foot control panel connection ..................... 48Friction adjustment knob ............................. 59Fuses ......................................................... 202

GGas spring ................................................. 195Gray filter 25% .................................... 38, 202

HHalogen light source

Changing lamps .................................... 192Control elements .................................... 64

HaMode filter ...................................... 38, 202Handgrips.............................................. 55, 57

Configuration........................................ 147HD DigiZoom............................................. 161HD video

Viewing ................................................ 168HD videos

Deleting................................................ 171HD-SDI video output.................................... 48

Hue ............................................................. 87

IIDIS ............................................................. 85Illumination intensity ................................... 24Image format............................................... 87Image inversion

Configuration........................................ 148Functionality ........................................... 83

Incision/LRI .................................................. 86Instrument tray ............................................ 46Integrated 22" monitor................................ 45Integrated HD camera ................................. 86Integrated HD video and image recording ... 87Integrated keratoscope ring......................... 46

Function status ..................................... 160Integrated protection filters ......................... 24integrated slit illumination ........................... 86

Function status ..................................... 157Slit position............................................. 86Slit width ................................................ 86

Integrated slit illuminatorRotary knob ............................................ 55

Intended use................................................ 15Interpupillary distance

Adjusting .............................................. 116Adjustment wheel................................... 56

Invertertube E .............................................. 41Adjustment wheel................................... 56Image inversion .................................... 148

KK TRACK...................................................... 85

LLamp change............................................... 38Language .................................................. 133Letterbox................................................... 141Light guide input ......................................... 47Light source

Halogen.................................................. 37LED......................................................... 37Status ..................................................... 54Superlux Eye ........................................... 37

Limiting downward travel ............................ 60Links............................................................ 84

Configuration........................................ 151Locking tab.................................................. 43

Instructions for Use Keyword indexOPMI LUMERA 700

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MMagnetic brake ..................................... 39, 60Magnetic coupling, eyepieces ...................... 41Main menu

Tab 1 ...................................................... 71Tab 2 ...................................................... 72

Maintenance12 months ............................................ 1792 years.................................................. 1814 years.................................................. 1816 months .............................................. 1796 years.................................................. 181

Manual mode .............................................. 84Manual mode switch ................................... 61Maximum exposure times

Integrated slit illuminator ........................ 28Red reflex illumination ............................ 27Surrounding field illumination ................. 28

Maximum radiation exposure ...................... 27Medical Device Directive ............................ 201Mobility

Monitor mount ..................................... 197Suspension arm .................................... 196

Multilayer T* super anti reflection coating.. 177

NNetwork connection .................................. 202

Default settings..................................... 142Establish via switch ................................. 94Establishing............................................. 96LAN 1 ..................................................... 48LAN 2 ..................................................... 48

Normal use .................................................. 15

OObjective lens .............................................. 42Operating personnel .................................... 16Operating sequence................................... 174OPMI light ................................................... 81Overhead display ................................... 40, 53

Configuration........................................ 150Light intensity display.............................. 53

PPatient file ................................................. 165Peak / average ............................................. 87Photos

Deleting................................................ 171Recording ............................................. 167

Viewing ................................................ 170Phototoxic damage................................ 20, 22Phototoxic injury

Measures ................................................ 24Potential equalization .................................. 48Power inlet socket ....................................... 48Power outlet................................................ 48Power switch............................................... 61Preconfigured button assignments

Foot control panel .................................. 75Handgrip................................................. 73

Product modifications.................................. 17Protection class.......................................... 202Protection filters .......................................... 24

RRated frequency ........................................ 202Rated voltage ............................................ 202Red reflex illumination ................................. 81Red value..................................................... 87Remote connection ............................. 48, 202Reset options............................................... 83

Configuration........................................ 152RESIGHT 700

Internal focus speed................................ 83Two-step speed ...................................... 83

RESIGHT functionAssigning .............................................. 136Functionality ........................................... 79

RESIGHT functions ....................................... 83Retina protection filter ................... 24, 38, 202RHEXIS ........................................................ 86RoHS compliance....................................... 201

SSafety inspection ....................................... 181SCI illumination...................................... 26, 81

Function status ............................. 155, 156Mix ratio ......................................... 54, 153Rotary knob ............................................ 55Status ..................................................... 54

Service menu ............................................. 198Setting the date......................................... 138Setting the illumination.............................. 153Setting the time......................................... 138Sidecut ...................................................... 141Slit position.................................................. 86Slit width ..................................................... 86Speed

Focus, zoom, XY coupling..................... 149

Keyword index Instructions for UseOPMI LUMERA 700

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RESIGHT 700 internal focus................... 149Stand base................................................... 43Stand column .............................................. 44Status bar .................................................... 65Steerable casters.......................................... 43Storage location .......................................... 88Strain relief ................................................ 104Superlux Eye light source

Changing .............................................. 194Control elements .................................... 64

Support arm .......................................... 36, 44Integrated 22" monitor ........................... 45

Surgery profileCreating................................ 133, 134, 135Deleting................................................ 138

Surgical microscopeControl elements .................................... 54Device description................................... 40

Surrounding field illumination...................... 81Suspension arm ........................................... 39

TTarget group ............................................... 15Technical specifications.............................. 202

Video outputs ....................................... 203Tilting device ............................................... 54Total current consumption......................... 202Total magnification.............................. 82, 157Transport handle ......................................... 44

UUSB port...................................................... 48User language ........................................... 133Users

Creating................................................ 132Deleting................................................ 133

VVideo

Recording ............................................. 166Status ..................................................... 53

Video formatSDTV..................................................... 141

Video log and OS licenses ............................ 88Video log files............................................ 146Video outputs.............................................. 48Video quality ............................................... 88

WWeight balancing ........................................ 60White balance ........................................... 161Widefield eyepiece....................................... 41Work area ................................................... 65

XXY coupling................................................. 39

Initial position ......................................... 59Inversion ............................................... 149

XY reset button ........................................... 59

YY/C video output (green).............................. 48YPbPr video output...................................... 49

ZZ ALIGN....................................................... 85Zoom

Assistant's microscope ............................ 56Surgical microscope ................................ 55

Carl Zeiss Meditec AG

Goeschwitzer Strasse 51-52

07745 Jena

Germany

Internet: www.zeiss.com/med

E-mail: [email protected]

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