SCHEDULE : GEN2016

EQUIPMENT : INFUSION PUMP

QUANTITY :

NO

SPESIFIKASI

1 GENERAL

1.1

Compact electric pump which used to administers and controls the

infusion solution as specified and thus provides as wide range of

applications for infusion therapy.

1.2 The infusion pump must be safe and accurate for use.

1.3 It must be user friendly and easy to operate safely.

2 FEATURE

2.1 Its shall be compatible to current existing IV set in KKM (e.g IV sets of 20

drops/ml or 60 drops/ ml). Vendor to provide documentation

2.2 Uses drop sensor to control drip rate of IV fluid and detect irregularities in

drop count (if applicable)

2.3 The delivery rate can be set as drop count (drop/min) or volumetric flow

rate (ml/hr).

2.4 User friendly inclined panel and colour coded major setting keys for easy

visual confirmation.

2.5 Key lock function for safety

3 TECHNICAL SPECIFICATION

3.1 Should be used with universal IV Infusion set provided by KKM (can be

used with gravity and pump IV set). Vendor to provide certification.

3.2 A wide range can be supported:

a) Micro drip 0.1-99.9ml/hr.

b) Macro drip 1-999ml/hr.

4 ALARMS

4.1 Audible and visual alarms with alarm sounds.

4.2 Alarm sounds when the AC power is turned off and the unit is switched to

battery operation.

4.3

Alarms alert for empty container, occlusion, door open, air in line, low

battery, infusion complete, drop sensor connection, unregulated flow and

other device malfunction.

5 DIMENSION AND WEIGHT

5.1 This pump must be light weight and easy to handle.

6 POWER REQUIREMENT

6.1 AC Power: 100-240V.

6.2 Built in rechargeable battery: 12V, minimum for 4 hours battery back up.

6.3 External DC:DC 12-15V.

7 STANDARD ACCESSORIES

7.1 IV Drip set x 10 units

7.2 Drop sensor (if applicable)

7.3 Pole clamp.

7.4 AC Power cord according to Malaysia Standard x 1 unit

7.5 Manual and services Operation Guide x 2 units

8 WARRANTY AND SERVICE

8.1 One year warranty against manufacturing defects upon successful

testing & commissioning. Preventive Maintenance will be provided twice

during warranty period.

9 USER TRAINING

9.1 User training on the operation and maintenance of the unit will be

provided.

10 DELIVERY

10.1 The equipment shall be delivered to the respective hospital listed in

Lampiran 1.

10.2 Delivery shall be within 8- 12 weeks from the date of LPO

EQUIPMENT: SYRINGE PUMP WITH DRUG CALCULATIONS ( TYPE A)

QUANTITY:

NO

SPESIFICATION

1 GENERAL

1.1 Compact electric pump which used to administers and controls the infusion solution as

specified and thus provides as wide range of applications for infusion therapy in critical area.

1.2 The infusion pump must be safe and accurate for use.

1.3 It must be user friendly and easy for nurses to operate safely.

1.4 It must have provision for at least one decimal point.

1.5 The display for parameter settings must be very clearly marked to avoid reading mistakes.

1.6 The engagement of syringe must be simple and fast.

1.7 It must be light weight (less than 2.5 kg).

2 APPLICABLE

2.1 It shall also be able to take different size syringes (10 ml, 20 ml, 30 ml and 50 ml).

2.2 The syringe detection shall be automatic.

2.3 The unit shall support universal syringe used in KKM.

2.4 It shall have a body weight drug calculation mode.

3 VOLUME LIMIT SETTING

3.1 0.1- 999 ml.

4 FLOW RATE RANGE

4.1 It should be delivered from 0.1 ml to 99.9 ml/hr.

5 FLOW RATE CHANGE DISPLAY

5.1 It shall display change by 0.1 ml/hr.

5.2 Shall allow dosage to be changed while continuing infusion.

6 PURGE RATE

6.1 Must allow for controlled bolus administration. Vendor to specify the rate.

7 OCCLUSION DETECTION

7.1 This pump must be very efficient in detecting occlusions with multiple level pressure limit adjustment

7.2 There must be selectable occlusion pressure level suitable for use in newborn.

8 ALARM SYSTEM There must be audio-visual alarm for the followings:

8.1 Occlusion.

8.2 Overload.

8.3 Infusion completion/empty syringe.

8.4 Low battery.

8.5 Clutch disengagement.

8.6 Syringe disengagement.

8.7 Power failure-power loss, power off malfunction.

9 POWER REQUIREMENT

9.1 AC power: 100-240V.

9.2 External DC: DC 12-15V.

9.3 Built-in rechargeable battery: 12V, with a minimum of 4 hours back-up battery.

The system must be operable even while recharging.

9.4 The pump shall be: diathermy and/or high frequency current-proof.

10 STANDARD ACCESSORIES

10.1 Syringe 50 ml x20 units.

10.2 Pole clamp x1 unit.

10.3

AC Power cord x1 unit. Power cord must be of the current Malaysian standard.

10.4 Operation and service manual x2 units.

11 WARRANTY AND SERVICE

11.1 One year / twelve (12) months warranty against manufacturing defects upon successful

testing & commissioning. Preventive maintenance will be provided twice during the

warranty period.

12 USER TRAINING

12.1 User training on the operation and maintenance of the unit will be provided.

13 DELIVERY

13.1 8-12 weeks from the date of LPO.

● Bold are mandatory

NO. UNIT1 1

a. 7" TFT wide view angle display with resolution of 1280 x 800 pixelsb.c.d.

e.

f.

g.

h.i.

j. Preview button for the images and videos captured is available.k.

l.

2. 1

--

-

Monitor pixels

Integrated with a slot to store SD memory card, hence it allows documentation of still images (JPEG) and video (MPEG4) into the SD memory card

Easy to use touch keys, for instants operation even during difficult circumstances

The metallic connector end is designed for intuitive insertion into the system interface on CMOS device

Digital cable with length of 2 meters

Connecting Cable

Battery Display Width

Input VoltagePower consumption

Features

: 100-240VAC, 50/60 Hz: 130g

Display HeightLine Voltage Weight of adaptor

: 5V: 12VA: Lithium Ion, 3.6V 4300mA: 154mm: 93mm

SPECIFICATION FOR VIDEOLARYNGOSCOPES (COMPLETE SET)

DESCRIPTION 7" TFT Monitor

: 1280 x 800 pixels: 1050gm

Cable with two male connectors at both ends: Metallic one is for CMOS device with system interface and the other connector is for monitor

Features:

Splash proof according to IP54 - suitable for wipe disinfectionResistant ABS plastic housing thus can withstand heavy loads

Must be able to mount of the IV drip stand

Technical specification :

Video output for connecting external monitor - good for teaching purposes

Operating with line voltage and rechargeable lithium ion batteries, operating time 2 hours

Soft keys button enable for the setting of the brightness, color contrast, hue based on user preference

The SD memory card must be easily removed and its USB port simplifies data transfer for further documenting.Must be able to connect with the video laryngoscope, flexible video intubation scope and also the single chip C-CAM camera head.

: 155mm: IP54: IEC Class II

Light weightHeightWidthWater protectionClassification

: 230mm

-

-

-

3 1- Special curved blade shape for difficult intubation- Ergonomics designed handle- Blade tips of all blade types visible for safe navigation- CMOS technology with LED illuminaton-

-

4 1

5 Guide for blades 1-

- package of 10

6 Flexible Intubation Video Endoscope (FIVE - 5.5mm) 1

Features :------- Possible to exchange flexible scope and video laryngoscopes in seconds

Video Imaging in 4:3 format provides better view

- 8 pin connector to CMOS processor / monitor

Manual/machine cleaning and disinfection, sterilization with Steris, AMSCO V-PRO 1, Sterrad (50S. 100S, 200S, NX, 100NX) and ETO gas; High-Level Disinfection (HLD) according to US Standards.

Suitable and validated for the following reprocessing methods up to 93°C:

Waterproof and fully immersible for cleaning and disinfection according to IPX8

Ergonomically designed handle

Connection

Videolaryngoscope blade (For difficult intubation - adult)

With system interface, documentation of images and video sequences via BlueButton

High Image resolutionLightweight

Compatible with Blade and Blade-HUBCompact design

Magill Forceps - AdultMAGILL Forceps, modified by BOEDEKER, length 25 cm, suitable for endoscopic foreign body removal, for use with video laryngoscopes size 2 - 4

: 200cm

For use with Connecting Cable for monitor or processor as well as pocket monitor

Special GUIDE, guide rod made of stainless steel with atraumatic tip, distal region is adapted to the blade shape of the video laryngoscope BLADE, fixation of endotracheal tube with the integrated tube holder possible

Plug diameter

Connecting Cable

- metallic connector to CMOS device: 8 mm

Length

Technical Specification

- 3 buttons on the handle for documentations and white balance purpose-

--

-

Technical Specifications for Flexible Intubation Video Endoscope 5.5mm 1- CMOS Technology- With suction channel- Deflection up/down : 140deg/140deg- Direction of view : 0 deg- Angle of view : 85deg- Working length : 65cm- Total length : 93cm- : 2.3mm

- Distal tip outer diameter : 5.5mm- Weight : 385g

Accessories included:i. Plug for luer-lock connectorii. Irrigation adaptoriii. Suction Valveiv. Bronchoscope insertion tube, size 4v. Bronchoscope insertion tube, size 2vi. Tube Holdervii. Caseviii. Pressure compensation capix. Leakage testerx. Cleaning Brushxi. Protection cap

7 Videolaryngoscope Trolley 1

-- Stainles steel tray 30cmx20cmx10cm-

8 1-----

High Level Disinfection (HLD) acc. to US standard

Integrated LED light source

Working channel inner diameter

Suitable and validated for the following low-temperature reprocessing methods up to max 60 celciusManual/machine cleaning and disinfection, sterilization with Sterrad®, EtO gas

Trolley consist of:Rollable with five legs and antistatic castors

1 Flexible scopes holder

Must be able to use with VIP trolley

Proshield Protective Tube for FlexiblescopesFor flexible scopes protectionSingle useDistal closedPackage of 10

BORANG JADUAL PEMATUHAN SPESIFIKASI BARUJABATAN ANESTESIOLOGY AND INTENSIVE CAREPERALATAN INTENSIVE CARE VENTILATORSKUANTITI 40 UNIT

BIL MANDATORY1 YES NO

1.1 √2

2.1

2.1.1 √

2.1.2 √

2.1.3 √

2.1.4 √

2.1.5 √

2.1.6 √

2.1.7 √

2.1.8 √

2.1.9 √

Pressure Regulated Volume Control or equivalent

Airway Pressure Release Ventilation (APRV)/Bi-Level/ BIPAP or equivalent

Non Invasive Positive Pressure Ventilation (NIPPV) with leak compensation

COMPLIANCE (tick /)

TENDERER VALUE / DETAIL

APPLICATIONTECHNICAL SPECIFICATIONS

To provide various modes of ventilatory support in critical care areas for infants, paediatrics and adult patients.

Ventilatory modes shall include:Control/ Assist Control/ Continuous Mandatory Ventilation (CMV)

Synchronized Intermittent Mandatory Ventilation (SIMV)

Continuous Positive Airway Pressure (CPAP) or equivalent

Pressure Control Ventilation (PCV)

SPECIFICATIONS

Volume Control Ventilation ( VCV) with option of constant and decelerating flow

Pressure Support (PS)

DOCUMENTATION PROVE REMARK

DOKUMEN B

KOD PENTENDER

KOS0NGKAN

2.22.2.12.2.22.2.32.2.42.2.5

a.b.

2.2.6

2.2.7

2.2.8

2.2.9

2.2.10

2.3

2.3.1

2.3.2

2.3.3

2.3.4

2.3.52.4

2.4.1 √

2.4.2

2.4.3 √

a. √

b. √

c. √

d. √

e. √

f. √

g. √

h. √

i. √

j. √

k. √

l. √

m. √

n. √

o. √

2.4.4 √

Peak Inspiratory Flow

Wave Forms and Flow Patterns

Rapid Shallow Breathing Index or equivalent

Respiratory maneuvers. Measured parameters should be clearly displayed:

Breath Rate

Inspiratory: Expiratory time

Inspired Oxygen Concentration

Peak Airway Pressure

Mean Airway Pressure

Plateau Pressure

Pressure Support level

CPAP Level

PEEP Level

Peak inspiratory flow

Expired Tidal Volume

Expired Minute Volume

Spontaneous Minute Volume

Inspired oxygen concentration (FiO2) of 21%-100%

Trigger sensitivity shall include both flow and pressure trigger

Positive End Expiratory Pressure up to at least 40 cmH2O

Pressure Support in the range 0 to 60 cmH20

Inspiratory Pressure of at least 50 cmH2O

CPAP of up to 25 cmH2O

Set Respiratory Rate from 1 to 50bpm

Apnea backup to be available

Max flow not less than 140L/minInspiratory time: Expiratory time ratio

For non-invasive ventilation (NIPPV) the following features shall be available:Shall automatically compensate for leakage through mask – vendor to specify the value

Operator set variables shall include at least:

Min flow 1L/min

Tidal Volume of at least 10-1500mls

Display of the parameters:

All set and delivered parameters shall be stated in offer letter.

Fully integrated display panel of set and delivered parameters on a single LCD touch screen of at least 12 inches in size

Parameters to be shown- breath by breath monitoring display of the following datas

CMV breath rate 0-80/minSIMV breath rate 0-40/minPeak Inspiratory Pressure 5 – 100 cmH2O

a. √

b. √

c. √

d. √

2.5 √

2.5.1 √

2.5.2 √

2.5.3 √

2.5.4 √

2.5.5 √

2.5.6 √

2.5.7 √

2.5.8 √

2.5.9 √

2.5.10 √

2.5.11 √

2.5.12 √

2.6

2.6.1 √

2.6.2 √

2.6.3

2.6.4

2.6.5

2.6.6

a.

b.

c.

2.6.7

2.6.8

a.

b.

c.

d.

e.

f.2.7

Hose heating wire in the inspiratory limb

Breathing circuits – reusable and autoclave (silicone material)-including water traps and y piece (with temperature probe port)

Two sets each of adult and paediatric circuit

Disposable circuit for adult x 100 sets/unit

Disposable circuit for pediatric x 20 sets/unit

Hot water heater/bath variety servo controlled.

Adjustable inspired gas temperature

Airway temperature digital display

High and low temperature alarm

Autoclavable chamber/housing heater hose chamber

Disposable bacterial and viral filters at inspiratory and expiratory each limbs x 200pcs/unit

Humidifier:

Power requirement:

Disconnection

Loss of PEEP

Technical error

Heavy duty compressor– guarantees continuous ventilation for continuous long operation hours when central gas supply not available

Internal battery at least 3 hours of ventilation for emergency backup in case of an electrical power supply failure

High quality mobile pedestal mounted on high quality castor

Hinged support arm with circuit support ‘Y’

Colour coded gas hoses with water traps and appropriate pipelineprobes, minimum length of 4 meters

Essential Component

High Airway Pressure

Low/ High Expired Minute Volume

Low/ High Tidal Volume

Apnea alarm with backup ventilation

Low / High End Expiratory Pressure

High continuous pressure

Oxygen concentration (FiO2)

Ventilator alarm functions:

Gas/power supply failure

Inspiratory Hold

Expiratory Hold

P 0.1 or Equivalent

Negative Inspiratory Pressure or equivalent

Audible alarm with different colour intensity

2.7.1

2.7.2

2.7.3

2.8

2.8.1

2.8.2

The power supply shall comply to the local requirements, rules and regulations

240V/50-60Hz with battery back up

Driving gas compressed air at 50-60psi/oxygen 50-60psi

STANDARD ACCESSORIES

Accessories necessary to complete a fully functional system should be supplied

Inclusive of stand-alone ultrasonic nebulizer 1 unit per hospital

3

3.1

3.2

3.3

3.4 √

3.5 √

3.6 √

3.7 √4

4.14.1.14.1.2

4.1.35 √

5.1

√5.2

√5.3

√5.4

√5.5

√5.6

√5.7

√6

6.1

√

7

7.1 √

7.1.1 √

7.1.2 √

Technical support shall be provided by the expertise for the period of 36 months, during warranty period

On site 24hrs

Vendor is able to provide replacement unit at no cost in the event of a downtime within 1 week during warranty period

Respond time: Via phone 2hrs

WARRANTY AND PPM SERVICES

All equipment supplied shall be guaranteed for a minimum period of 36 months following satisfactory installation, commissioning and handing over.

The vendor shall state and provide details of general and specific guarantees.

Relevant information on the particular model of equipment offered shall be stated.

The equipment shall also conform to other approved National Standards (Medical Device Act 2012) with regards to the design, construction, performance and tests.

All equipment supplied shall in all relevant respects conform to the current editions of all relevant Malaysia Standards, Medical Device Act 2012, British Standards, IEC-601 or other approved National Standards with regards to the design, construction, performance and tests. A copy of such standards in English Language shall be submitted with the bid.

Where applicable, the vendor shall submit copies of all relevant and pertinent approvals standards on safety and efficacy.

Unless otherwise indicated, all units of measurement shall be Standard International Units

Unless otherwise indicated, all units of measurement shall be Standard International Units

SUPPORT

SAFETY

The machine comes with over pressure valve

The machine comes with active exhalation valve

Vendor to specify others

Full information & supporting documents:

The vendor shall provide list of technical support personnel in the event of machine breakdown.

The vendor shall guarantee the availability of spare parts for a period of 10 years after satisfactory handing over of the equipment. A certificate from the manufacturer shall accompany each offer.

TRAINING Clinical on-site training by qualified clinical application personnel for a minimum of 5 working days for each unit yearly (to be decided by the end user).

OTHER REQUIREMENT

Maintenance shall be available also on weekends.The vendor shall provide 6 monthly (6 times) comprehensive maintenance service & quality assurance program during the warranty period.The vendor must assure a reliable & prompt after sales service.

7.1.3 √

7.2 √

7.2.1 √

7.2.2 √

7.3 √

8

8.1 √

8.2 √

99.1 √9.2 √

The equipment shall be compatible and shall be provided with the Clinical Information System to be linked/interface with existing network (where applicable) in hospital - the cost of integration between the equipment and existing network must be borne by the equipment vendor

The vendor shall validate and substantiate all information provided in the offer either through original catalogues or other verified literature. Failure to do so may result in the offer being rejected without further clarification or enquiry.

Checklist and Offer Document (borang tawaran / spesifikasi):

The delivery (including T&C) shall be completed AS SOON AS POSSIBLE. Failure to comply will lead to penalty imposed.

The bidder shall prepare a checklist of all pertinent equipment features stated in the above specifications with columns denoting their offer/s' conformance with the requirements. Where the checklist denotes non-conformance with the stated requirements, bidders are advised to append notes and comments explaining why such an offer may be deemed equivalent or superior to those in the requirements.

Bids maybe rejected if the checklist and/or the offer document/s are incomplete. Bids maybe rejected if the supporting documents are incomplete.

The Equipment shall be delivered to HOSPITAL-HOSPITAL KEMENTERIAN KESIHATAN MALAYSIA listed in Lampiran 1

PACKAGE CONFIGURATION

User manual x 2Service manual x 2END SPECIFICATION

DELIVERY

:

:

:

TECHNICAL SPECIFICATIONS NOTES / REFERENCEYES NO

1 DESCRIPTION

1.1The patient monitor is used for monitoring and display the physiological parameters of patients.

2 MANDATORY REQUIREMENTS

2.1Item offered that do not fullfill all the mandatory requirements below shall be rejected

2.2 The monitor must be a MODULAR type multichannel monitor

2.3Integrated transport monitor module, which shall also be able to work as a standalone multiparameter Monitor.

2.4 Capable of : 2.4.1 NIBP2.4.2 SpO22.4.3 ECG2.4.4 Heart Rate2.4.5 Respiration2.4.6 Temperature2.4.7 Invasive BP2.4.8 ETCO2 monitoring

2.5

Dedicated Central Monitoring Systems with networking must be provided for the monitors at the Emergency Department Red Zone and Neonatal ICU (NICU)

3 ESSENTIAL FEATURES 3.1 Modular Patient Monitoring

3.1.1Compact Multiparameter module intergrate to most frequent used parameters into a single unit

3.1.2 Selectable Neonatal, Paediatric or Adult patient mode

3.1.3 High Resolution capacitative touchscreen display of at least 17 inch size

3.1.4 Waveform Channels: minimum 10-waveform channels.

3.1.5 Capable of multiple onscreen display modes

3.1.6

Abilty to view-other- patient function enables clinician to view other monitor on the same network at bedside where they are working.

3.1.7 Able to print reports on the recorder or to a network printer

3.1.8Main Unit shall provide power backup with rechargeable Lithium-ion battery at least runs for 2 hour.

3.2 Transport Modular (Mini Monitor)

3.2.1The main monitor shall integrate a modular monitor, which shall also be able to work as a standalone transport monitor.

3.2.2 Shall have a colour LCD screen of at least 5 inch

3.2.3 The monitor shall display up to 4 channels of waveforms

COMPLIANCEBIL

SCHEDULE

EQUIPMENT

QUANTITY

CRITICAL PATIENT MONITOR WITH CENTRAL MONITORING SYSTEM 8 PARAMETER NIBP, SPO2, HR, TEMP. ECG, RESP,IBP, ETCO2

3.2.4The transport module shall has a built in Lithium Ion battery supports at least 5 hours of continous monitoring

3.2.5 The modular monitor shall be compact and easy to carry, weigh less than 1000gram

3.2.6

The modular monitor shall provide integrated WiFi network to facilitate seamless connections during transport. The WiFi shall comply with IEEE 802.11 a/b/g/n standard and works at both 2.4G and 5G frequency ranges.

3.2.7 The transport monitor shall comply with EN1789 or equivalent for free fall protection

3.2.8The patient data and measurement records shall remain stored in the Patient Monitor when electric power is off.

3.3 Data Storage and Review

3.3.1

Permanent Data Storage: the patient data and measurement records shall remain stored permanently in the Patient Monitor even after electric power down and battery depleted.

3.3.2 At least 48 hours of full disclosure waveforms and numeric data

3.3.3 At least 120 hours of tabular and graphic trends

3.4 Network and Transfer

3.4.1

Network: the Monitor shall support layer 3 communications and automatic DHCP IP address allocation for both wired and wireless networks.

3.4.2 Wire Network: the Monitor shall provide IEEE 802.3 RJ45 network interface.

3.4.3

Wireless Network: the Monitor shall provide integrated Wi-Fi network. It shall be compatible with IEEE 802.11 a/b/g/n at both 2.4GHz and 5GHz operating frequency. Standard WPA2-Enterprise encryption shall be provided for Wi-Fi data security.

3.4.4

Data Transfer: the patient monitor shall have data transfer capability for transferring patient demographic, tabular and graphic trends, alarm setting, and events to other monitors.

3.5 NIBP

3.5.1Accurate reading of NIBP in the presence of motion artifact using motion-tolerant technology or equivalent

3.5.2 Technique: Oscillometric, using stepwise deflation pressure

3.5.3 Operation mode: Manual, Automatic interval, STAT

3.6 SPO2

3.6.1 The monitor must use a motion-tolerant signal processing FAST SpO2 algorithm.

3.6.2SpO2 monitoring with advanced technology for accuracy under conditions of low perfusion

3.7 ECG

3.7.1 Capable of 3, 5 and 12 lead ECG monitoring

3.7.2 Able to perform 12 Lead ECG at the bedside

3.7.3 Automatic pacemaker detection

3.7.4 Capable of arrythmia analysis for adult, pediatric, and neonate.

3.7.5 Capable of ST segment analysis

3.8 Respiration3.8.1 Technique: Trans-thoracic impedance

3.9 ETCO2

3.9.1 Sidestream with changeable water trap on the ETCO2 module

3.10 Clinical Assistance Application

3.10.1

The unit shall have built-in software and fully integrated to provide checklist to help doctor operate and treat following Surviving Sepsis Campaign (SSC) guideline.

4

CENTRAL MONITORING SYSTEM - Vendor to supply 2 Systems and to be installed at Emergency Department Red Zone and Neonatal Intensive Care Unit

4.1 Capable of connecting at least 16 monitors.

4.2Supports individual bed frequency setup in each telemetry monitoring system. Supports multi-screen display mode.

4.3Capable of displaying information from 16 monitors in the single-screen mode and 32 monitors in the multi-screen mode.

4.4 Allows to view a single patient.

4.5Supports networking between multiple CentralStations and remote CentralStations.

4.6 Able to review up to 240 hours of trend data for each online patient.

4.7 Able to review up to 720 events for each online patient.

4.8 Provides audible and visual alarms.

4.9

Provides the functions of drug calculations, titration table calculations, hemodynamics calculations, oxygenation calculations, ventilation calculations and renal calculations.

4.10 Provides the ability to record, print and save data.

4.11 Provides comprehensive help information, prompts and operational guidance.

4.12Supports such peripherals as the keyboard, touchscreen, mouse, thermal recorder, laser printer, speaker, etc.

4.13 Supports wired and wireless network.

4.14 Provides data output meeting the HL7 protocol.

4.15Supports receiving the data generated during interruption from networked monitors and combining the data.

5 ESSENTIAL ACCESSORIES SUPPLIED PER MONITOR :

5.1 Patient ECG Leads:5.1.1 1X 3 Lead ECG cables, clip type

5.2 NIBP:5.2.1 1 x Pressure Interconnect hose5.2.2 1 x NIBP Cuff Neonate5.2.3 1 x NIBP Cuff Child 5.2.4 1 x NIBP Cuff Small Adult 5.2.5 1 x NIBP Cuff Adult 5.2.6 1 x NIBP Cuff Large Adult 5.2.7 1 x NIBP Cuff Thigh

5.3 Pulse Oximeter:5.3.1 1X Reusable Adult Finger SpO2 Sensor5.3.2 1X Reusable Child Finger SpO2 Sensor5.3.3 1X Reusable Neonate SpO2 Sensor

5.4 Temperature:5.4.1 1 x Reusable Temperature probe, Skin

5.5 CO2:5.5.1 Water Trap: 1 box (10pcs/box)5.5.2 Sampling Line: 1 packet (10pcs/pkg)

5.6 IBP:

5.6.1 IBP startup kits with 10 x IBP Disposable Transducer

5.7 1X Bed rail hook5.8 1X Wall mount

6 ADDITIONAL ESSENTIAL ACCESSORIES SUPPLIED (TOTAL):

6.1 6 X 12-Leads ECG cable

6.2 6 x Reusable Temperature probe, Oesophageal/rectal, Adult

6.3 8 x Reusable Temperature probe, Oesophageal/rectal, Pediatric

7 Essentials for Central Monitoring System

7.1 1 x CPU with build in USB port each department

7.2 2 x 19" TFT Touch screen display each department

7.3 1 x Audio card and Speaker each department

7.4 1 x Keyboard and Mouse each department

7.5 1 x Windows 7 Workstation operating system each department

7.6 1 x Central station application software each department

7.7 1 x Laserrjet Printer & Thermal Recorder Module each department

7.8 1 x Uninterruptible Power Supply (UPS) each department

8 STANDARD REQUIREMENTS & INSTRUCTIONS

8.1 The equipment should be supplied fully installed and made fully functioning.

8.2 Service and operating manual and original catalogue in English should be provided.

8.3

2 years device warranty from the day of the testing and commissioning of the monitor with a of minimum 2 PPM in first year of warranty

8.4

On-site training by application specialist and factory trained personnel on operation, clinical applications, running self-test and basic trouble shooting.

8.5Local technical expertise available for the maintenance and repair of the particular model of equipment offered .

8.6 Full information & supporting documents:

8.6.1 Relevant information on the particular model of equipment offered shall be stated.

8.6.2

The equipment shall also conform to other approved National Standards (Medical Device Act 2012) with regards to the design, construction, performance and tests.

8.6.3

The vendor shall validate and substantiate all information provided in the offer either through original catalogues or other verified literature. Failure to do so may result in the offer being rejected without further clarification or enquiry.

8.6.4 Checklist and Offer Document (borang tawaran / spesifikasi):

8.6.4.1

The bidder shall prepare a checklist of all pertinent equipment features stated in the above specifications with columns denoting their offer/s' conformance with the requirements. Where the checklist denotes non-conformance with the stated requirements, bidders are advised to append notes and comments explaining why such an offer may be deemed equivalent or superior to those in the requirements.

8.6.4.2

Bids maybe rejected if the checklist and/or the offer document/s are incomplete. Bids maybe rejected if the supporting documents are incomplete.

9 DELIVERY

9.1 The complete systems shall be delivered (including T&C)

9.2 The Equipment shall be delivered to

10 PACKAGE CONFIGURATION 10.1 User manual x 210.2 Service manual x 2

END SPECIFICATION