invacare® perfecto₂₂₂™oxygen concentrator® perfecto₂ oxygen concentrator 1.2 intended...

Invacare® Perfecto₂₂₂™OxygenConcentratorIRC5PO2, IRC5PO2W, IRC5P, IRC5PW

en HomeFill® System CompatibleUser Manual

This manual MUST be given to the user of the product.BEFORE using this product, read this manual and save for future reference.

©2016 Invacare®CorporationAll rights reserved. Republication, duplication or modification in whole or in part is prohibited withoutprior written permission from Invacare. Trademarks are identified by ™and ®. All trademarks areowned by or licensed to Invacare Corporation or its subsidiaries unless otherwise noted.Making Life’s Experiences Possible is a trademark in the U.S.A.Pine-sol and Lestoil are registered trademarks of The Clorox Company.Dawn is a registered trademark of The Proctor and Gamble Company.

Contents

1 General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41.1 Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41.2 Intended Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61.3 Indications For Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61.4 Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71.5 Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

2 Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82.1 Label Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82.2 General Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 92.3 Radio Frequency Interference . . . . . . . . . . . . . . . . . . . . . . 12

3 Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 133.1 Component Identification . . . . . . . . . . . . . . . . . . . . . . . . . 133.2 Pneumatic Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

4 Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 164.1 Optional Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

5 Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 175.1 Unpacking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 175.2 Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 175.3 Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

6 Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 186.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 186.2 Select a Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 186.3 Setting Up the Concentrator . . . . . . . . . . . . . . . . . . . . . . 196.3.1 Setting Up the Humidifier . . . . . . . . . . . . . . . . . . . . . . 196.3.2 Turning the Concentrator On . . . . . . . . . . . . . . . . . . . 216.3.3 Flowrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 216.3.4 SensO2 Oxygen Purity Indicator . . . . . . . . . . . . . . . . . 226.3.5 Units without SensO2 . . . . . . . . . . . . . . . . . . . . . . . . 23

7 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 247.1 Service Life . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 247.2 Cleaning the Cabinet . . . . . . . . . . . . . . . . . . . . . . . . . . . . 247.3 Cleaning the Cabinet Filter . . . . . . . . . . . . . . . . . . . . . . . . 257.4 Humidifier Cleaning and Thermic Disinfection . . . . . . . . . . 257.5 Cleaning and Disinfection Between Patients . . . . . . . . . . . . 267.6 Preventive Maintenance Checklist . . . . . . . . . . . . . . . . . . . 27

8 After Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 288.1 Recycling Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . 288.2 Wear and Tear . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28

9 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 299.1 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

10 Technical data. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3110.1 Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31

11 Warranty. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3411.1 North American Limited Warranty . . . . . . . . . . . . . . . . . 34

Invacare® Perfecto₂™Oxygen Concentrator

1 General

1.1 SymbolsSignal words are used in this manual and apply to hazards or unsafepractices which could result in personal injury or property damage.See the information below for definitions of the signal words.

DANGER!– Danger indicates an imminently hazardous situationwhich, if not avoided, will result in death or seriousinjury.

WARNING!– Warning indicates a potentially hazardous situationwhich, if not avoided, could result in death or seriousinjury.

CAUTION!– Caution indicates a potentially hazardous situationwhich, if not avoided, may result in property damageor minor injury or both.

Gives useful tips, recommendations and information forefficient, trouble-free use.

Symbols in Documentation

General Warning Sign

The background color inside thetriangle is yellow on product labels.

Read manual

The color of the symbol backgroundis blue on product labels.

No Smoking

The color of the circle with diagonalbar is red on product labels.

No Open Flame

The color of the circle with diagonalbar is red on product labels.

Class II, Double Insulated

Protected against solid foreign objects of 12.5mm diameter and greater.

Protected against vertically falling water drops.

Indoor Use ONLY

Keep Dry

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General

-20FMIN

150FMAX

Transport and Storage Temperature

15%MIN

95%MAX Transport and Storage Humidity

Alternating Current

Type BF equipment

Recycle

DO NOT dispose of in household waste

Electrical Hazard

Manufacturer

Call supplier

Symbols on Product

Unit running

Unit not running

O2 Indicators

Symbol O2 Purity Indicator Lights (LED)

O2 SYSTEMOKAY

O2 over 85%

GREEN Indicator Light

O2 between73% to 85%

YELLOW Indicator Light

A. YELLOW Solid

B. YELLOW Flashing Sensor

Failure. Call a qualified technician

SYSTEMFAILURE

O2 Below 73%

RED Indicator Light

Refer to Troubleshooting.

LX Indicators

Symbol O2 Purity Indicator Lights (LED)

I/O SYSTEMOKAY

GREEN Indicator Light

SYSTEMFAILURE

RED Indicator Light

Continuous Audible Alarm Sieve —GARD™

Compressor Shutdown

Call a qualified technician.

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1.2 Intended UseThe intended function and use of the Invacare® Perfecto₂™OxygenConcentrator is to provide supplemental oxygen to patients withrespiratory disorders, by separating nitrogen from room air, by wayof a molecular sieve. It is not intended to sustain or support life.

DANGER!Risk of Injury or DeathThis product is to be used as an oxygen supplement andis not intended to be life-supporting or life-sustaining.ONLY use this product if the patient is capable ofspontaneous breath, able to inhale and exhale withoutthe use of a machine.– DO NOT use in parallel or series with other oxygenconcentrators or oxygen therapy devices.

DANGER!Risk of Injury or DeathDepending on their medical condition, patients on flowrates greater than 5 L/min may be at an increased riskfor serious injury or death in the event of failure.– ALWAYS discuss this increased risk with your healthcare supplier BEFORE using this product if you areprescribed a flow rate greater than 5 L/min.

WARNING!Risk of Injury or DamageUse of this product outside of the intended use andspecifications has not been tested and may lead toproduct damage, loss of product function, or personalinjury.– DO NOT use this product in any way other thandescribed in the Specifications and Intended Usesections of this manual.

DANGER!Risk of Injury or DeathWhile Invacare strives to produce the best oxygenconcentrator in the market today, this oxygenconcentrator can fail to produce oxygen due to powerfailure or device malfunction.– ALWAYS have a backup source of oxygen readilyavailable.

– In the event the concentrator fails to produce oxygen,the concentrator will briefly alarm signaling the patientto switch to their backup source of oxygen. Refer toTroubleshooting for more detail.

1.3 Indications For UseThe intended function and use of the Invacare® Perfecto₂™OxygenConcentrator is to provide supplemental oxygen to patients withrespiratory disorders, by separating nitrogen from room air, by wayof a molecular sieve. It is not intended to sustain or support life.

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General

1.4 DescriptionThe Invacare Perfecto2 concentrator is used by patients withrespiratory disorders who require supplemental oxygen. The deviceis not intended to sustain or support life.

The oxygen concentration level of the output gas ranges from 87%to 95.6%. The oxygen is delivered to the patient through the useof a nasal cannula.

The Invacare Perfecto2 concentrator uses a molecular sieve andpressure swing adsorption methodology to produce the oxygengas output. Ambient air enters the device, is filtered and thencompressed. This compressed air is then directed toward one oftwo nitrogen adsorbing sieve beds.

Concentrated oxygen exits the opposite end of the active sieve bedand is directed into an oxygen reservoir where it is delivered to thepatient.

The Invacare Perfecto2 concentrator is capable of operation by thepatient in a home environment or in an institutional environment.Device operates at a nominal 120 VAC/60 Hertz supply.

Service information will be available upon request to qualifiedtechnical personnel only.

1.5 ContraindicationsThere are no known contraindications.

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2 Safety

2.1 Label Locations

A

BSerial number label is located on the resonatorintake assembly.

CSpecification Label is located on the back of theconcentrator at the base.

D

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Safety

2.2 General GuidelinesIn order to ensure the safe installation, assembly and operation of theconcentrator these instructions MUST be followed.

DANGER!Risk Of Death, Injury, Or DamageImproper use of the product may cause death, injury ordamage. This section contains important information forthe safe operation and use of this product.– DO NOT use this product or any available optionalequipment without first completely reading andunderstanding these instructions and any additionalinstructional material such as user manuals, servicemanuals or instruction sheets supplied with thisproduct or optional equipment.

– If you are unable to understand the warnings, cautionsor instructions, contact a healthcare professional,dealer or technical personnel before attempting touse this equipment.

– Check ALL external components and carton fordamage. In case of damage, or if the product is notworking correctly, contact a technician or Invacarefor repair.

– THE INFORMATION IN THIS DOCUMENT ISSUBJECT TO CHANGE WITHOUT NOTICE.

DANGER!Risk Of Death, Injury, Or Damage From FireTextiles, oil or petroleum substances, grease, greasysubstances and other combustibles are easily ignitedand burn with great intensity in oxygen enriched air andwhen in contact with oxygen under pressure. To avoidfire, death, injury or damage:– DO NOT SMOKE while using this device.– DO NOT use near OPEN FLAME or IGNITIONSOURCES.

– DO NOT use any lubricants on concentrator unlessrecommended by Invacare.

– NO SMOKING signs should be prominently displayed.– Avoid creation of any spark near oxygen equipment.This includes sparks from static electricity created byany type of friction.

– Keep all matches, lighted cigarettes, electroniccigarettes or other sources of ignition out of theroom in which this concentrator is located and awayfrom where oxygen is being delivered.

– Keep the oxygen tubing, cord, and concentrator outfrom under such items as blankets, bed coverings,chair cushions, clothing, and away from heated or hotsurfaces including space heaters, stoves, and similarelectrical appliances.

CAUTION!Federal (statutory) law restricts this device sale to oron the order of a medical practitioner licensed by agovernmental agency where he/she practices.– ONLY a licensed medical practitioner may order thepurchase or use of this device.

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DANGER!Risk of Death, Injury, from Electric ShockTo reduce the risk of burns, electrocution, death orinjury to persons:– DO NOT disassemble. Refer servicing to qualifiedservice personnel. There are no user serviceableparts.

– Avoid using while bathing. If continuous usageis required by the physician's prescription, theconcentrator must be located in another room atleast 7ft (2.1m) from the bath.

– DO NOT come in contact with the concentratorwhile wet.

– DO NOT place or store concentrator where it candrop into water or other liquid.

– DO NOT reach for concentrator that has fallen intowater. Unplug IMMEDIATELY.

– DO NOT use frayed or damaged AC power cords.

WARNING!Risk Of Injury Or Damage– Invacare products are specifically designed andmanufactured for use in conjunction with Invacareaccessories. Accessories designed by othermanufacturers have not been tested by Invacare andare not recommended for use with Invacare products.

– There are many different types of humidifiers, oxygentubing, cannulas and masks that can be used with thisdevice. You should contact your local home caresupplier for recommendations on which of thesedevices will be best for you. They should also give youadvice on the proper usage, maintenance, and cleaning.

DANGER!Risk of Injury or DeathTo avoid choking or ingestion of chemicals from airwaycontamination:– DO NOT use the concentrator in the presence ofpollutants, smoke, fumes, flammable anesthetics,cleaning agents, or chemical vapors.

WARNING!Risk of Injury or DeathTo prevent injury or death from product misuse:– Closely supervise when this concentrator is used byor near children or impaired individuals.

– Monitor patients using this device who are unable tohear or see alarms or communicate discomfort.

WARNING!Risk of Injury or DeathTo avoid choking and/or strangulation from tubingentanglement:– Keep children and pets away from nasal cannula andtubing.

– Close supervision is necessary when the nasal cannulais used by or near children and/or impaired persons.

WARNING!Risk of Injury or DeathTo reduce the risk of injury or death from illness:– Replace the nasal cannula on a regular basis. Checkwith your equipment supplier or physician todetermine how often the cannula should be replaced.

– DO NOT share cannulas between patients.

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Safety

WARNING!Risk of InjuryA change in altitude may affect total oxygen available toyou. To prevent oxygen deprivation:– Consult your physician before traveling to higher orlower altitudes to determine if your flow settingsshould be changed.

WARNING!Risk of Injury or DamageTo prevent injury or damage from cord misuse:– DO NOT move or relocate concentrator by pullingon the cord.

– DO NOT use extension cords with AC power cordsprovided.

– Properly store and position electrical cords and/ortubing to prevent a tripping hazard.

WARNING!Risk of Injury or DamageTo prevent injury or damage from misuse:– NEVER leave concentrator unattended when pluggedin.

– Make sure concentrator is off when not in use.

WARNING!Risk of Injury or DamageInvacare oxygen concentrators are specifically designedto minimize routine preventive maintenance. To preventinjury or damage:– Only professionals of the healthcare field orpersons fully conversant with this process such asfactory trained personnel should perform preventivemaintenance or performance adjustments on theoxygen concentrator, except for tasks described inthis manual.

– Users should contact your dealer or Invacare forservice.

CAUTION!Risk of DamageTo prevent damage from liquid ingress:– If the concentrator is not working properly, if ithas been dropped or damaged, or dropped intowater, call equipment supplier/qualified technician forexamination and repair.

– NEVER drop or insert any object or liquid into anyopening.

– For indoor use ONLY.

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2.3 Radio Frequency Interference

WARNING!Risk of Injury or DamageTo reduce the risk of injury or product damage frominterference with wireless equipment:– Keep concentrator at least 9.8 ft (3.0 m) away fromwireless communication equipment such as wirelesshome network devices, mobile phones, cordlessphones and base stations, walkie-talkies, etc.

This equipment has been tested and found to comply with EMC limitsspecified by IEC/EN 60601-1-2. These limits are designed to providea reasonable protection against electromagnetic interference in atypical medical installation.

Other devices may experience interference from even the low levelsof electromagnetic emissions permitted by the above standards.To determine if the emissions from the concentrator are causingthe interference, turn the concentrator Off. If the interferencewith the other device(s) stops, then the concentrator is causing theinterference. In such rare cases, interference may be reduced orcorrected by one of the following measures:

• Reposition, relocate, or increase the separation between theequipment.

• Connect the equipment into an outlet on a circuit different fromthat to which the other device(s) is connected.

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Components

3 Components

3.1 Component Identification

A Oxygen Outlet

B Flowmeter

C Elapsed Time Meter

D Oxygen Purity IndicatorLights/Fault and Power IndicatorLights

E Circuit Breaker

F Power Switch

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Rear View

G Power Cord

H HomeFill Outlet Fitting

I Cabinet Filter

The HomeFill outlet fitting H is to be used only forfilling oxygen cylinders with the HomeFill home oxygencompressor. The outlet fitting does not affect concentratorperformance. Refer to the HomeFIll user manual, partnumber 1100873, for connection and operating instructions.When not in use, the plug provided with the concentratorshould be inserted into the outlet fitting. For moreinformation about the HomeFill, contact your Invacaredealer.

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Components

3.2 Pneumatic Diagram

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4 Accessories

4.1 Optional AccessoriesThere are many different types of humidifiers, oxygen tubing, cannulasand masks that can be used with this device. You should contact yourlocal home care provider for recommendations on which of thesedevices will be best for you. They should also give you advice on theproper usage, maintenance, and cleaning.

The supply accessories (nasal cannula, mask, tubing, humidifier, etc.)used to deliver oxygen to the patient need to include a means toreduce the propagation of fire in the accessories for the safety of thepatient and others. If a commercially available, fire-activated flowstop device is used in the accessories setup, it should be placed asclose to the patient as practicable.

The following optional accessories and replacement parts (listedbelow) are also available:

• Standard Adult Nasal Cannula, 7 ft (2.1 m) - M3120• Standard Humidifier - Invacare Part #1155719• PreciseRX™ Pediatric Flowmeter Accessory - IRCPF16• HomeFill Home Oxygen Compressor - IOH200• Oxygen Supply Tubing 7 ft (2.1 m) - MS4107• Oxygen Supply Tubing 21 ft (6.3 m) - MS4121• Oxygen Tubing Connector - MS4301

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Setup

5 Setup

5.1 Unpacking

1. Check for any obvious damage to the carton or its contents. Ifdamage is evident, notify the carrier, or your local dealer.

2. Remove all loose packing from the carton.3. Carefully remove all the components from the carton.

Unless the oxygen concentrator is to be usedIMMEDIATELY, leave concentrator in its packaging forstorage until use is required.

5.2 Inspection

1. Inspect/examine exterior of the concentrator for nicks, dents,cracks, scratches or other damage.

2. Inspect all components.

5.3 Storage

1. Store the repackaged oxygen concentrator in a dry area. Refer toTypical Product Parameters for storage temperature parameters.

2. DO NOT place objects on top of repackaged concentrator.

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6 Usage

6.1 IntroductionYour oxygen concentrator is intended for individual use indoors.It is an electronically operated device that separates oxygen fromroom air. It provides high concentration of oxygen directly to youthrough a nasal cannula. Clinical studies have documented thatoxygen concentrators are therapeutically equivalent to other types ofoxygen delivery systems.

Your provider will show you how to use your oxygen concentrator.He/She should be contacted with any questions or problemsregarding your oxygen concentrator. This user manual will tell youabout your concentrator and will serve as a reference as you useyour concentrator.

6.2 Select a Location

WARNING!Risk of InjuryTo avoid injury during therapy:– The oxygen concentrator MUST be placed on a levelsurface for use.

– DO NOT relocate the oxygen concentrator while inuse.

WARNING!Risk of Injury or DamageTo avoid injury or damage from airborne pollutantsand/or fumes and for optimal performance:– Locate and position the concentrator in a wellventilated space so that the air intake and the airexhausts are not obstructed.

– NEVER block the air openings of the concentratoror place it on a soft surface, such as a bed or couch,where the air opening may be blocked.

– Keep the openings free from lint, hair and similarforeign items.

– Keep concentrator at least 12 inches (30,5 cm) awayfrom walls, draperies and furniture.

– Avoid use in presence of pollutants, smoke or fumes,flammable anesthetics, cleaning agents or chemicalvapors.

– Place concentrator in a well ventilated area to avoidairborne pollutants and/or fumes.

– DO NOT use in a closet.

You may select a room in your house where using your oxygenconcentrator would be most convenient. Your concentrator can beeasily rolled from room to room on its casters.

Your oxygen concentrator will perform best when operated underthe conditions outlined in typical product parameters.

Usage in environments other than those described may result in theneed for increased equipment maintenance. The air intake of theunit should be located in a well ventilated area to avoid airbornepollutants and/or fumes.

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Usage

6.3 Setting Up the Concentrator

1. Plug in power cord to an electrical outlet.2. Connect Humidifier (if so prescribed).

6.3.1 Setting Up the Humidifier

WARNING!Risk of Injury or DamageTo avoid burns from steam or hot water, inhalation ofwater and/or water damage to the concentrator:– DO NOT fill humidifier bottle with hot water. Allowboiled water to cool to room temperature beforefilling.

– DO NOT overfill humidifier.– Replace the humidifier cap and securely tighten.Confirm that the cap is not cross-threaded on thehumidifier bottle.

– DO NOT reverse the oxygen input and outputconnections. Water from the humidifier bottle willtravel through the cannula back to the patient if inputand output connections are reversed.

– When using tubing connections longer than 7 ft(2.1 m) in length, position the humidifier as closeto the patient as possible to allow for maximumhumidification output.

WARNING!Risk of Injury or DamageFailure to properly install the humidifier bottle or otheraccessories to the concentrator will impact the flow ofoxygen.– To check for proper operation of the oxygenconcentrator and accessories, place the end of thenasal cannula under the surface of a half-full cup ofwater only when the oxygen is flowing and look forbubbles indicating proper operation. Wipe any excesswater off the nasal prongs when finished before placingon the patient.

– If there are no bubbles, check all connections(including humidifier bottle and other accessories, ifapplicable) and repeat. Contact your dealer or serviceprovider immediately if bubbles still do not appear.

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Humidifier Bottlewith Cap

Humidifier Bottle without Cap

1. Remove cap A from bottle B.2. Fill humidifier with boiled tap water or bottled water to the level

indicated by the manufacturer. Boil tap water for approximately10 minutes and cool to room temperature prior to use.

CAUTION!Risk of Damage– Confirm the humidifier cap is not cross-threadedon the humidifier bottle.

3. Insert a flathead screwdriver in the plate groove on the top edgeof the filter access door C and gently pry the filter access dooroff.

4. Pull up and remove the humidifier bottle adapter D.

5. Attach the humidifier bottle adapter to the humidifier bottle byturning the wing nutE on the humidifier bottle counterclockwiseuntil it is securely fastened.

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Usage

6. Select the location for the humidifier bottle/adapter assembly:

• When placing the humidifier bottle in the compartment Fon the concentrator, attach the humidifier bottle/adaptertube Gto the oxygen outlet connector H on theconcentrator.

When using tubing connections longer than 7 ft (2.1 m)in length, position the humidifier as close to the patientas possible to allow for maximum humidification output.

7. Attach the patients’ nasal cannula supply tube to the humidifierbottle outlet.

8. After assembly, ensure that oxygen is flowing through the nasalcannula.

6.3.2 Turning the Concentrator On

1. Press power switch A to On position.

All the panel lights and the audible alarm will comeon for one second, confirming that the indicators arefunctioning properly.

6.3.3 Flowrate

WARNING!Risk of InjuryTo avoid injury from excess oxygen or a deficit ofoxygen:– DO NOT change the L/min setting on the flowmeterunless a change has been prescribed by your physicianor therapist.

Do not set the flow above the RED ring. An oxygen flowgreater than 5 L/min will decrease the oxygen concentration.

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1. Turn the flowrate knob A to the setting prescribed by yourphysician or therapist.

To properly read the flowmeter B, locate theprescribed flowrate line on the flowmeter. Next, turnthe flow knob until the ball C rises to the line. Now,center the ball on the L/min line prescribed.

2. If the flowrate on the flowmeter ever falls below 0.5 L/min D formore than about one minute, the Potential Obstruction Alertwill be triggered. This is a rapid beeping of the audible alarm.Check your tubing or accessories for blocked or kinked tubingor a defective humidifier bottle. After rated flow is restored tobetween 0.5 L/min and 0.75 L/min, the Potential ObstructionAlert will turn off.

A Potential Obstruction Alert indicates a conditionthat may be associated with a partial or completeobstruction of oxygen output.

The use of some accessories such as thePreciseRx™Pediatric Flowmeter and the HomeFillcompressor will deactivate the Potential ObstructionAlert.

6.3.4 SensO2 Oxygen Purity IndicatorThis feature monitors the purity of oxygen generated by the oxygenconcentrator. If purity falls below factory preset standards, indicatorlights on the control panel will illuminate.

Initial Startup of the ConcentratorConcentrator may be used during the initial warm-up time(approximately 30 min.) while waiting for the O2 purity toreach maximum.

When the unit is turned on, the GREEN light will come on (SYSTEMOK/O2 greater than 85%). After five minutes, the oxygen sensor willbe operating normally and will control the indicator lights dependingon oxygen concentration values.

Explanation of Oxygen Purity Indicator Lights

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Usage

SymbolO2

Purity

IndicatorLight(LED)

Explanation

A O2

SYSTEMOKAY O2

over 85%

GREENlight

No action isneeded. Normalfor operation.

YELLOWlight (Solid)

B

O2

between73% and85%

YELLOWlight

flashing

Immediately callsupplier. You maycontinue to use theconcentrator unlessinstructed otherwiseby your supplier. Becertain that backupoxygen is nearby.

C

SYSTEMFAILUREO2 below73%

RED light(Solid)

Continuous AudibleAlarm

Sieve-GARD™CompressorShutdown

SYSTEM FAILURE.Total unit shutdown.Immediately switchto backup oxygensupply and callsupplier.

D — — Call Supplier

6.3.5 Units without SensO2

Concentrator may be used during the initial start warm-uptime (approximately 30 min). O2 purity will build to amaximum during this period.

Light Symbol Explanation

AGREENlight

Normal Operation

BREDlight

Continuous Audible Alarm

Sieve-GARD™Compressor

Total unit shutdown. Immediatelyswitch to backup oxygen supplyand call supplier.

C — Call Supplier

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7 Maintenance

7.1 Service Life

WARNING!Risk of Injury or DamageUse of the product beyond this time period may causeproduct damage and injury.– This product has an expected lifetime of three(3) years when used in accordance with safetyinstructions, maintenance intervals and correct usestated in this manual.

– Perform all maintenance according to therecommended schedule in this manual.

The effective product lifetime can vary according tofrequency and intensity of use.

7.2 Cleaning the Cabinet

DANGER!Risk of Injury or DamageInvacare oxygen concentrators are specifically designedto minimize routine preventive maintenance. To preventinjury or damage:– Only qualified personnel should perform preventivemaintenance on the oxygen concentrator.

– DO NOT remove cabinet.

DANGER!Risk of Injury or DamageLiquid will damage the internal components of theconcentrator. To avoid damage or injury from electricalshock:– Turn Off the concentrator and unplug the power cordbefore cleaning.

– DO NOT allow any cleaning agent to drip inside theair inlet and outlet openings.

– DO NOT spray or apply any cleaning agent directlyto the cabinet.

– DO NOT hose down the product.

CAUTION!Risk of DamageHarsh chemical agents can damage the concentrator.To avoid damage:– DO NOT clean the cabinet or filter with alcoholand alcohol based products (isopropyl alcohol),concentrated chlorine-based products (ethylenechloride), and oil-based products (Pine-Sol®, Lestoil®)or any other harsh chemical agents. Only use mildliquid dish detergent (such as Dawn®).

At a minimum, preventive maintenance MUST be performedaccording to the maintenance record guidelines. In placeswith high dust or soot levels, maintenance may need tobe performed more often. Refer to the PreventativeMaintenance Checklist.

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Maintenance

Periodically clean the concentrator’s cabinet as follows:

1. Use a damp cloth, or sponge, with a mild detergent such asDawn dish washing soap to gently clean the exterior case.

2. Allow the concentrator to air dry, or use a dry towel, beforeoperating the concentrator.

7.3 Cleaning the Cabinet Filter

CAUTION!Risk of DamageTo avoid damage to the internal components of the unit:– DO NOT operate the concentrator without the filterinstalled or with a dirty filter.

There is one cabinet filter located on the back of the cabinet.

1. Remove the filter and clean as needed.

Environmental conditions that may require morefrequent inspection and cleaning of the filter include, butare not limited to: high dust, air pollutants, etc.

2. Clean the cabinet filter with a vacuum cleaner or wash with amild liquid dish detergent (such as Dawn™) and water. Rinsethoroughly.

3. Thoroughly dry the filter and inspect for fraying, crumbling, tearsand holes. Replace filter if any damage is found.

4. Reinstall the cabinet filter.

7.4 Humidifier Cleaning and ThermicDisinfection

Clean and disinfect the oxygen humidifier daily to reducelimestone deposits and eliminate possible bacterialcontamination. Follow the instructions provided by themanufacturer. If none are provided, follow these steps:

1. Wash humidifier in soapy water and rinse with a solution of tenparts water and one part vinegar.

2. Rinse thoroughly with hot water.3. Air dry thoroughly.

To limit bacterial growth, air dry the humidifier thoroughlyafter cleaning when not in use. Refer to Set Up for use.

1143482-H-00 25


7.5 Cleaning and Disinfection Between Patients

WARNING!Risk of Injury or DamageTo prevent injury from infection or damage toconcentrator:– Only qualified personnel should perform cleaningand disinfection of the oxygen concentrator andaccessories between patients.

Follow these instructions to eliminate possible pathogenexchange between patients due to contamination ofcomponents or accessories. Preventive Maintenance shouldalso be performed at this time if necessary.

1. Dispose of and replace all patient side accessories not suitablefor multiple patient use, including but not limited to:

• Nasal Cannula and Tubing• Mask• Humidifier

2. Perform maintenance procedures described in this manual anditems on Preventive Maintenance Checklist

3. Check concentrator for possible external damage or signs that itmay require service or repair.

4. Ensure concentrator functions properly and all alarms are inworking order.

5. Before repackaging and distribution to new patient, ensurepackaging contents contain the concentrator and user manual.

26 1143482-H-00

Maintenance

7.6 Preventive Maintenance Checklist

Model No: Serial No:

ON EACH INSPECTION

Record Date of Service

Record Elapsed Hours on Hour Meter

Clean Cabinet Filter(s) (Refer to Cleaning the Cabinet Filter.)

Check Prescribed L/min. Flow Rate

DURING PREVENTIVE MAINTENANCE SCHEDULE, OR BETWEEN PATIENTS

UNITS WITHOUT SensO2 — Every 6 months of continuous use (Equivalent to 4,380 hours)

Check Oxygen Concentration (green indicator light)

Clean/Replace Cabinet Filter(s) (Refer to Cleaning the Cabinet Filter.)

Check/Replace Outlet HEPA Filter*

Check/Replace Compressor Inlet Filter*

Check Power Loss Alarm*

UNITS WITH SensO2 — Every 3 years of continuous use (Equivalent to 26,280 hours)

Check Oxygen Concentration (green indicator light)

Clean/Replace Cabinet Filter(s) (Refer to Cleaning the Cabinet Filter.)

Check/Replace Outlet HEPA Filter*

Check/Replace Compressor Inlet Filter*

Check Power Loss Alarm*

*To be conducted by provider or qualified service technician. Refer to service manual.

1143482-H-00 27


8 After Use

8.1 Recycling InformationThis product may contain substances that could be harmful to theenvironment if disposed of in places (landfills) that are not appropriateaccording to legislation.

Follow local governing ordinances and recycling plans regardingdisposal of the concentrator or components normally used inoperation. The concentrator does not generate waste or residue inoperation.

• DO NOT dispose of the concentrator in the normal wastestream.

• Any accessories not part of the concentrator MUST be handledin accordance with the individual product marking for disposal.

8.2 Wear and TearInvacare reserves the right to ask for any item back that has analleged defect in workmanship. See Warranty that shipped with theproduct for specific warranty information.

Refer to the User Manual for proper preventative maintenanceschedule and use of the product.

This is just a general guideline and does not include items damageddue to abuse and misuse.

Normal wear and tear items and components for this product arelisted below.

• All types of filters• All types of tubing

Sieve is a porous filtering material and is considered a wearitem. Some factors that could affect sieve material life includehumidity, temperature, particulates, air contaminates, airintake, vibration and other environmental conditions.

28 1143482-H-00

Troubleshooting

9 Troubleshooting

9.1 Troubleshooting

SYMPTOM PROBABLE CAUSE SOLUTION

Alarm: Main Power Loss:

No lights illuminated.

Short Beeps, long pause

Concentrator not operating,power switch On.

Beep...Beep...

1. Power cord not plugged in.2. No power at outlet.3. Tripped circuit breaker.

1. Insert plug into outlet.2. Inspect house circuit breakers or fuses. If problem recurs,

use a different outlet.3. Push/reset circuit breaker. If problem recurs, call service

provider.

Alarm: System Failure:

RED light illuminated.

Continuous

Concentrator not operating,power switch On.

Beep...

1. Unit overheating due to blockedair intake.

2. Insufficient power at outlet.3. Internal repairs required.

1. Do one or both of the following:

a. Remove and clean cabinet filters.b. Move oxygen concentrator at least 12 in (30, 5 cm)

away from walls, draperies or furniture.

2. DO NOT use extension cords. Move to another electricaloutlet or circuit.

3. Call service provider.

1143482-H-00 29


SYMPTOM PROBABLE CAUSE SOLUTION

Alarm: Potential Obstruction Alert

GREEN light illuminated.

Rapid

Beep...Beep...

Beep...Beep

1. Possible internal obstruction in theoxygen path. Kinked or blockedtubing, cannula or humidifier.

2. Flowmeter set at 0.5 L/min or less.

1. Inspect for kinks or blockages. Correct, clean or replaceitem. Once corrected, turn power Off for 60 seconds andthen turn power back ON.

2. Reset flowmeter to prescribed flowrate. If prescribedflowrate is below 0.5 L/min, use the Pediatric FlowmeterIRCPF16 (Only with Perfecto2 5).

The use of the pediatric flowmeter will deactivate thePotential Obstruction Alert.

Alarm: System Failure:

YELLOW* or RED lightIlluminated.

Alarm: Continuous On RED light

* Only applies toIRC5PO2

1. Low oxygen purity.*2. Kinked or blocked tubing, cannula

or humidifier.*3. Flowmeter set at 0.5 L/min or less*.4. Unit overheating due to blocked

air intake.5. Insufficient power at outlet.6. Internal repairs required.

1. Clean or Replace filters.2. Inspect for kinks or blockages. Correct, clean or replace

item. Once corrected, turn power Off for 60 seconds andthen turn power back On.

3. Check flowmeter is set to 1.0 L/min or more. Refer toTypical Product Parameters.

4. Do one or both of the following:

a. Remove and clean cabinet filters.b. Move concentrator at least 12 in (30,5 cm) from walls,

draperies, and furniture.

5. DO NOT use extension cords. Move to another electricaloutlet or circuit.

6. Call Service Provider.

GREEN light with YELLOW LightFlashing.

1. Internal repairs required. 1. Call Service Provider.

30 1143482-H-00

Technical data

10 Technical data

10.1 Specifications

Electrical Requirements: 120 VAC + 10, –15% (132 VAC/102 VAC), 60 Hz

Rated Current Input: 3 A

Sound Level: 43 ± 2 dBA Average for Perfecto2 Models

40 ± 2 dBA Average for Perfecto2W Models

Altitude: All Perfecto2 Models:Up to 8,000 ft (2438 m) above sea levelwithout degradation of concentration levels.

All Perfecto2 Models while filling a HomeFill System:Up to6,000 ft (1828 m) above sea level without degradation of concentrationlevels.

Atmospheric Pressure Range: 101.3 kPa – 75.0 kPa

Oxygen Output Concentration Levels: 87% to 95.6% at 0.5 to 5 L/min

Concentration levels achieved after initial warm-up period(approximately 30 minutes)

Maximum Outlet Pressure: 5 psi ± 0.5 psi (34.5 kPa ± 3.45 kPa)

Low Flow Alarm: 0.5 to 5 L/min (maximum). For flowrates less than 1 L/min, werecommend the use of the Invacare Pediatric Flowmeter Accessory(IRCPF16).

Potential Obstruction Alert: 0 L/min to 0.5 L/min

The concentrator detects a condition that may indicate a potentialobstruction of the output oxygen. Rapid audible beeping alert (this alertis deactivated when accessories are connected). May be associatedwith flow setting of 0.5 L/min or less.

1143482-H-00 31


Power Consumption: 280 W (Operating at 3 L/min)

Pressure Relief Mechanism Operational at: 30 psi to 45 psi (207 kPa to 310 kPa )

Change in maximum recommended flow when back pressure of 7kPa isapplied:

0.7 L/min (Back Pressure of 7kPa applied)

Filters: Cabinet, Outlet HEPA and Compressor Inlet

Safety System: Current overload or line surge shutdown.

High temperature compressor shutdown.

High Pressure Alarm with compressor shutdown.

Low Pressure Alarm with compressor shutdown.

Battery Free Power Loss Alarm.

SensO2 Oxygen System.

Possible Obstruction Alert.

Width: 15 in ± 3/8 in (38.1 cm ± 1 cm)

Height: 23 in ± 3/8 in (58.4 cm ± 1 cm)

Depth: 12 in ± 3/8 in (30.5 cm ± 1 cm)

Weight: Perfecto2 Models - 43 lbs ± 2 lbs (19.5 kg ± 1 kg)

Perfecto2W Models – 45 lbs ± 2 lbs (20.5 kg ± 1 kg)

Shipping Weight: Perfecto2 Models – 48 lbs ± 2 lbs (21.8 kg ± 1 kg)

Perfecto2W Models - 50 lbs ± 2 lbs (22.7 kg ± 1 kg)

Operating Ambient Temperature and Humidity: Perfecto2 Models – 50°F - 95°F (10°C - 35°C) at up to 60% relativehumidity

Perfecto2W Models – 50°F - 90°F (10°C - 32°C) at up to 60% relativehumidity

32 1143482-H-00

Technical data

Cabinet: Impact Resistant flame-retardant plastic cabinet that conforms to UL94V–0

Standards and Regulatory Listing: Double Insulated Product ETL certified complying with UL1431 andUL1097 ETL certified to CSA C22.2 No. 68.

Electrical: No extension cords

Placement: No closer than 12 in (30.5 cm ) from any wall, furniture, draperies orsimilar surfaces to assure sufficient air flow.

Avoid deep pile carpets and heaters, radiators or hot air registers.

Floor location only.

No confined spaces (Example: No closets).

Tubing: 7 ft (2 m) cannula with a maximum 50 ft (15 m) of Crush-Proof Tubing

(DO NOT pinch)

Time of Operation: Up to 24 hours per day

Recommended Storage and Shipping Temperature: -20° F to 150° F (-29° C to 65° C) at up to 95% relative humidity

Measurement uncertainty is included in the device specification. All conditions at ATPD.

1143482-H-00 33


11 Warranty

11.1 North American Limited WarrantyTHE WARRANTY BELOW HAS BEEN DRAFTED TO COMPLY WITHFEDERAL LAW APPLICABLE TO PRODUCTS MANUFACTUREDAFTER JULY 4, 1975.

This warranty is extended only to the original purchaser whopurchases this product when new and unused from InvacareCorporation or a dealer. This warranty is not extended to anyother person or entity and is not transferable or assignable to anysubsequent purchaser or owner. Coverage under this warranty willend upon any such subsequent sale or other transfer of title to anyother person. This warranty gives you specific legal rights and youmay also have other legal rights which may vary from state to state.

Invacare Corporation warrants its Perfecto2 Oxygen Concentratorswhen purchased new and unused to be free from defects in materialsand workmanship for a period of three years from date of purchasefrom Invacare or a dealer, with a copy of the seller’s invoice requiredfor coverage under this warranty.

DO NOT OPEN OR ATTEMPT TO SERVICE THE 4-WAY VALVEBODY.

This will void any and all warranty applicable to the valve body. Ifwithin such warranty periods any such product shall be proven toInvacare Corporation's satisfaction to be defective, such productshall be repaired or replaced, at Invacare Corporation's option.This warranty only applies to the labor for repairs performed bythe Invacare Service Department or Invacare Authorized ServiceCenters. It does not apply to the labor performed by the purchaseror user. This warranty does not include normal wear and tear orshipping charges. Invacare Corporation's sole obligation and your

exclusive remedy under this warranty shall be limited to such repairor replacement.

Routine maintenance items, such as filters, are excluded fromthis warranty. For warranty service, please contact InvacareCorporation's Service Department at the toll free number on theback cover. Upon receiving notice of an alleged defect in a product,Invacare Corporation will issue a serialized return authorization.It shall then be the responsibility of the purchaser to return theentire unit or remove, at purchaser's cost, the defective componentpart(s) identified, pack the component part(s) in a manner to avoidshipping damage and to ship the component part(s) to eitherInvacare Corporation's plant or service center as specified byInvacare Corporation in advance. Defective component part(s)must be returned for warranty inspection using the serial numberas identification within thirty days of return authorization date. Donot return products to our factory without prior consent. C.O.D.shipments will be refused; please prepay shipping charges.

LIMITATIONS AND EXCLUSIONS: THE FOREGOINGWARRANTY SHALL NOT APPLY TO PRODUCTS SUBJECTEDTO NEGLIGENCE, ACCIDENT, IMPROPER OPERATION,MAINTENANCE OR STORAGE, SOOT OR SMOKE-FILLEDENVIRONMENTS, OR OTHER THAN NORMAL APPLICATION,USE OR SERVICE, OR TO PRODUCTS MODIFIED WITHOUTINVACARE CORPORATION'S EXPRESS WRITTEN CONSENT(INCLUDING, BUT NOT LIMITED TO, MODIFICATIONTHROUGH THE USE OF UNAUTHORIZED PARTS ORATTACHMENTS) OR TO PRODUCTS DAMAGED BY REASONOF REPAIRS MADE TO ANY COMPONENT WITHOUT THESPECIFIC CONSENT OF INVACARE CORPORATION ORTO PRODUCTS DAMAGED BY CIRCUMSTANCES BEYONDINVACARE CORPORATION'S CONTROL.

34 1143482-H-00

Warranty

THE FOREGOING EXPRESS WARRANTY IS EXCLUSIVE AND INLIEU OF ANY OTHER WARRANTIES WHATSOEVER, WHETHEREXPRESS OR IMPLIED, INCLUDING THE IMPLIED WARRANTIESOF MERCHANTABILITY AND FITNESS FOR A PARTICULARPURPOSE, AND THE SOLE REMEDY FOR VIOLATIONS OF ANYWARRANTY WHATSOEVER, SHALL BE LIMITED TO REPAIR ORREPLACEMENT OF THE DEFECTIVE PRODUCT PURSUANT TOTHE TERMS CONTAINED HEREIN. THE APPLICATION OF ANYIMPLIED WARRANTY WHATSOEVER SHALL NOT EXTENDBEYOND THE DURATION OF THE EXPRESS WARRANTYPROVIDED HEREIN. INVACARE SHALL NOT BE LIABLE FOR ANYCONSEQUENTIAL OR INCIDENTAL DAMAGES WHATSOEVER.

SOME STATES DO NOT ALLOW THE EXCLUSION ORLIMITATION OF INCIDENTAL OR CONSEQUENTIAL DAMAGE,OR LIMITATION OF HOW LONG AN IMPLIED WARRANTYLASTS, SO THE ABOVE EXCLUSION AND LIMITATIONMAY NOT APPLY TO YOU. THIS WARRANTY SHALL BEEXTENDED TO COMPLY WITH STATE/PROVINCIAL LAWSAND REQUIREMENTS.

1143482-H-00 35

Invacare Corporation

USA

One Invacare Way Elyria, Ohio USA 44035Tel: 440–329–6000 Tel: 800–832–4707 Technical ServicesTel: 440-329-6593Tel: 800-832-4707 www.invacare.com

Manufacturer

Invacare Corporation2101 E. Lake Mary Blvd.Sanford, FL 32773Tel: 407–321–5630

Manufacturer

Invacare RehabilitationEquipment (Suzhou) Co., Ltd.No. 5 Weixi Road, SIP,Suzhou, Jiangsu, PRC 215121Tel: 86–512–62586180Fax: 86–512–62586167

1143482-H-00 2016-08-02

*1143482H-00*Making Life’s Experiences Possible™

invacare® perfecto₂₂₂™oxygen concentrator® perfecto₂ oxygen concentrator 1.2 intended...

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