Invacare® Platinum® Oxygen

Concentrator
IRC9LXO2AWQ

en HomeFill® System Compatible

User Manual

This manual MUST be given to the user of the product.

BEFORE using this product, this manual MUST be read and saved for
future reference.
© 2022 Invacare Corporation
All rights reserved. Republication, duplication or modification in whole or in part is prohibited
without prior written permission from Invacare. Trademarks are identified by ™ and ®. All trademarks
are owned by or licensed to Invacare Corporation or its subsidiaries unless otherwise noted.
Platinum is a registered trademark in the U.S.A., Europe and Australia.
Making Life’s Experiences Possible is a registered 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.
 6.3.8 Elapsed Time Meter (Hour Meter) . . . . . . . . . . . . . . . 27
Contents
7 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
7.1 Service Life . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
1 General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 7.2 Cleaning the Cabinet . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
1.1 Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 7.3 Cleaning the Cabinet Filter . . . . . . . . . . . . . . . . . . . . . . . 29
1.2 Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 7.4 Humidifier Cleaning and Thermic Disinfection. . . . . . . . . . 31
1.3 Indications For Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 7.5 Cleaning and Disinfection Between Patients . . . . . . . . . . . 31
1.4 Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 7.6 Preventive Maintenance Checklist . . . . . . . . . . . . . . . . . . 32
1.5 Contraindications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 8 After Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
2 Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 8.1 Recycling Information . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
2.1 Label Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 8.2 Wear and Tear . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
2.2 General Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 9 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
2.3 Radio Frequency Interference . . . . . . . . . . . . . . . . . . . . . 13
9.1 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
3 Components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
10 Technical Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
3.1 Component Identification . . . . . . . . . . . . . . . . . . . . . . . . 14
10.1 Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
3.2 Pneumatic Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
10.2 Electromagnetic Compliance (EMC) . . . . . . . . . . . . . . . . 39
4 Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
11 Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
4.1 Optional Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
11.1 Customer Service and Warranty Information . . . . . . . . . 44
5 Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
5.1 Unpacking. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
5.2 Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
5.3 Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
6 Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
6.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
6.2 Select a Location. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
6.3 Setting Up the Concentrator . . . . . . . . . . . . . . . . . . . . . . 19
6.3.1 Setting Up the Humidifier (If Prescribed) . . . . . . . . . . 19
6.3.2 Connecting/Positioning the Nasal Cannula . . . . . . . . . 22
6.3.3 Turning the Concentrator On . . . . . . . . . . . . . . . . . . . 24
6.3.4 Flowrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
6.3.5 SensO2 Oxygen Purity Indicator . . . . . . . . . . . . . . . . . 26
6.3.6 Initial Startup of the Concentrator . . . . . . . . . . . . . . . 26
6.3.7 Explanation of Oxygen Purity Indicator Lights . . . . . . . 26
Invacare® Platinum® Oxygen Concentrator

1 General Symbols in Documentation

General Warning Sign
1.1 Symbols The background color inside the
Signal words are used in this manual and apply to hazards triangle is yellow on product labels.
or unsafe practices which could result in personal injury or
property damage. See the information below for definitions Read Manual
of the signal words.
The color of the symbol background
DANGER! is blue on product labels.
– Danger indicates an imminently hazardous
situation which, if not avoided, will result in No Smoking
death or serious injury. The color of the circle with diagonal
bar is red on product labels.
WARNING!
– Warning indicates a potentially hazardous No Open Flame
situation which, if not avoided, could result in
death or serious injury. The color of the circle with diagonal
bar is red on product labels.
CAUTION!
Class II, Double Insulated
– Caution indicates a potentially hazardous
situation which, if not avoided, may result in
property damage or minor injury or both. Protected against solid foreign objects of 12.5
mm diameter and greater.
Gives useful tips, recommendations and information
for efficient, trouble-free use. Protected against vertically falling water
drops.

Indoor Use ONLY

4 1195054-C
 General

**This product complies with Directive

Keep Dry 93/42/EEC concerning medical devices.
The launch date of this product is stated in
65C
MAX
Transport and Storage Temperature the CE declaration of conformity.
-29C EC Representative
MIN

95%
MAX Transport and Storage Humidity Reference Number
15%
MIN

Serial Number
Alternating Current

Type BF equipment
Symbols on Product
Unit running
Recycle
Unit not running
DO NOT dispose of in household waste
O2 Indicators
Electrical Hazard
Symbol O2 Purity Indicator Lights (LED)
O2 SYSTEM OKAY GREEN Indicator Light
Manufacturer
O2 over 85%

Call supplier

1195054-C 5
Invacare® Platinum® Oxygen Concentrator

O2 between 73% to YELLOW Indicator Light DANGER!

85% Risk of Injury or Death
A. YELLOW Solid Depending on their medical condition, patients
B. YELLOW Flashing on flowrates greater than 5 L/min may be at an
Sensor increased risk for serious injury or death in the
event of failure.
Failure. Call a qualified – ALWAYS discuss this increased risk with your
technician. health care supplier BEFORE using this product
SYSTEM FAILURE RED Indicator Light if you are prescribed a flowrate greater than
5 L/min.
O2 Below 73% Refer to Troubleshooting.
WARNING!
1.2 Intended Use Risk of Injury or Damage
Use of this product outside of the intended use
The intended function and use of the Invacare Platinum and specifications has not been tested and may
Oxygen Concentrator is to provide supplemental oxygen to lead to product damage, loss of product function,
patients with respiratory disorders, by separating nitrogen or personal injury.
from room air, by way of a molecular sieve. It is not – DO NOT use this product in any way other than
intended to sustain or support life. described in the Specifications and Intended
Use sections of this manual.
DANGER!
Risk of Injury or Death
This product is to be used as an oxygen
supplement and is not intended to be
life-supporting or life-sustaining. ONLY use this
product if the patient is capable of spontaneous
breath, able to inhale and exhale without the use
of a machine.
– DO NOT use in parallel or series with other
oxygen concentrators or oxygen therapy
devices.

6 1195054-C
 General

DANGER! Concentrated oxygen exits the opposite end of the active

Risk of Injury or Death sieve bed and is directed into an oxygen reservoir where it
While Invacare strives to produce the best oxygen is delivered to the patient.
concentrator in the market today, this oxygen
The Invacare Platinum concentrator is capable of operation
concentrator can fail to produce oxygen due to
by the patient in a home environment or in an institutional
power failure or device malfunction.
environment. Device operates at a nominal 230 VAC/50
– ALWAYS have a backup source of oxygen readily
Hertz supply.
available.
– In the event the concentrator fails to produce Service information will be available upon request to
oxygen, the concentrator will briefly alarm qualified technical personnel only.
signaling the patient to switch to their backup
source of oxygen. Refer to Troubleshooting for
more detail. 1.5 Contraindications
There are no known contraindications.
1.3 Indications For Use
To provide supplemental oxygen to patients with respiratory
disorders, by separating nitrogen from room air, by way of a
molecular sieve.
1.4 Description
The Invacare Platinum concentrator is used by patients with
respiratory disorders who require supplemental oxygen. The
device is 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 use of a nasal cannula.
The Invacare Platinum concentrator uses a molecular sieve
and pressure swing adsorption methodology to produce the
oxygen gas output. Ambient air enters the device, is filtered
and then compressed. This compressed air is then directed
toward one of two nitrogen adsorbing sieve beds.
1195054-C 7
Invacare® Platinum® Oxygen Concentrator

2 Safety Double insulation label is located on the back

C
of the concentrator at the base.
2.1 Label Locations IRC9LXO2AWQ

Serial number label is located on the

A
resonator intake assembly.
Specification label is located on the back of
B
the concentrator at the base.
2.2 General Guidelines
In order to ensure the safe installation, assembly and
operation of the concentrator, these instructions MUST be
followed.

8 1195054-C
 Safety

DANGER! DANGER!
Risk of Death, Injury or Damage Risk of Death, Injury or Damage from Fire
Improper use of the product may cause death, Textiles, oil or petroleum substances, grease,
injury or damage. This section contains important greasy substances and other combustibles are
information for the safe operation and use of this easily ignited and burn with great intensity in
product. oxygen enriched air and when in contact with
– DO NOT use this product or any available oxygen under pressure. Smoking during oxygen
optional equipment without first completely therapy is dangerous and is likely to result in
reading and understanding these instructions burns or death. To avoid fire, death, injury or
and any additional instructional material such damage:
as user manuals, service manuals or instruction – DO NOT SMOKE while using this device.
sheets supplied with this product or optional – DO NOT use near OPEN FLAME or IGNITION
equipment. SOURCES.
– If you are unable to understand the warnings, – NO SMOKING signs should be prominently
cautions or instructions, contact a healthcare displayed.
professional, dealer or technical personnel – Keep all open flames, matches, lighted
before attempting to use this equipment. cigarettes, electronic cigarettes or other sources
– Check ALL external components and carton for of ignition at least 10 ft (3 m) away from this
damage. In case of damage, or if the product concentrator or any oxygen carrying accessories
is not working correctly, contact a technician such as cannulas or tanks.
or Invacare for repair. – DO NOT allow smoking within the same room
– THE INFORMATION IN THIS DOCUMENT IS where the oxygen concentrator or any oxygen
SUBJECT TO CHANGE WITHOUT NOTICE. carrying accessories are located.
– If you disregard these warnings about the
severe hazard of oxygen use while you continue
to smoke, you must always turn off the
concentrator, remove the cannula and then
wait ten minutes before smoking or leave the
room where either the concentrator or any
oxygen carrying accessories such as cannulas
or tanks are located.

1195054-C 9
Invacare® Platinum® Oxygen Concentrator

DANGER! DANGER!
Risk of Death, Injury or Damage from Fire Risk of Death or Injury from Electric Shock
Textiles, oil or petroleum substances, grease, To reduce the risk of burns, electrocution, death
greasy substances and other combustibles are or injury to persons:
easily ignited and burn with great intensity in – DO NOT disassemble. Refer servicing to
oxygen enriched air and when in contact with qualified service personnel. There are no user
oxygen under pressure. Smoking during oxygen serviceable parts.
therapy is dangerous and is likely to result in – Avoid using while bathing. If continuous usage
burns or death. To avoid fire, death, injury or is required by the physician's prescription, the
damage: concentrator must be located in another room
– Use only oxygen compatible water-based lotions at least 2.1 m (7 ft) from the bath.
or salves before and during oxygen therapy. To – DO NOT come in contact with the concentrator
verify, refer to the lotion/salve container for while wet.
the oxygen compatible water-based statement. – DO NOT place or store concentrator where it
If necessary, contact the manufacturer. DO can drop into water or other liquid.
NOT use any lubricants on concentrator unless – DO NOT reach for concentrator that has fallen
recommended by Invacare. into water. Unplug IMMEDIATELY.
– Avoid creation of any spark near oxygen – DO NOT use frayed or damaged AC power
equipment. This includes sparks from static cords.
electricity created by any type of friction.
– Keep the oxygen tubing, cord, and concentrator
out from under such items as blankets,
bed coverings, chair cushions, clothing, and
away from heated or hot surfaces including
space heaters, stoves, and similar electrical
appliances.
– Turn the concentrator off when not in use to
prevent oxygen enrichment.

10 1195054-C
 Safety

WARNING! WARNING!
Risk of Injury or Damage Risk of Injury or Death
– Invacare products are specifically designed To prevent injury or death from product misuse:
and manufactured for use in conjunction with – Closely supervise when this concentrator is used
Invacare accessories. Accessories designed by by or near children or impaired individuals.
other manufacturers have not been tested by – Monitor patients using this device who are
Invacare and are not recommended for use unable to hear or see alarms or communicate
with Invacare products. discomfort.
– No modification of this equipment is allowed.
– There are many different types of humidifiers, WARNING!
oxygen tubing, cannulas and masks that can be Risk of Injury or Damage
used with this device. You should contact your To prevent injury or damage during use:
local home care supplier for recommendations – If you feel ill or uncomfortable, or if you are
on which of these devices will be best for you. unable to feel the oxygen flow, consult your
They should also give you advice on the proper equipment provider and/or your physician
usage, maintenance, and cleaning. IMMEDIATELY.

DANGER! WARNING!
Risk of Injury or Death Risk of Injury
To avoid choking or ingestion of chemicals from A change in altitude may affect total oxygen
airway contamination: available to you. To prevent oxygen deprivation:
– DO NOT use the concentrator in the presence – Consult your physician before traveling to
of pollutants, smoke, fumes, flammable higher or lower altitudes to determine if your
anesthetics, cleaning agents, or chemical flow settings should be changed.
vapors.

1195054-C 11
Invacare® Platinum® Oxygen Concentrator

WARNING! WARNING!
Risk of Injury or Damage Risk of Injury or Damage
To prevent injury or damage from cord misuse: Invacare oxygen concentrators are specifically
– DO NOT move or relocate concentrator by designed to minimize routine preventive
pulling on the cord. maintenance. To prevent injury or damage:
– DO NOT use extension cords with AC power – Only professionals of the healthcare field or
cord provided. persons fully conversant with this process such
– Properly store and position electrical cords as factory trained personnel should perform
and/or tubing to prevent a tripping hazard. preventive maintenance or performance
adjustments on the oxygen concentrator, except
WARNING! for tasks described in this manual.
Risk of Injury or Damage – Users should contact your dealer or Invacare
To prevent injury or damage from misuse: for service.
– NEVER leave concentrator unattended when
plugged in. CAUTION!
– Make sure concentrator is off when not in use. Risk of Damage
To prevent damage from liquid ingress:
CAUTION! – If the concentrator is not working properly, if
Risk of Minor Injury, Discomfort or Damage it has been dropped or damaged, or dropped
– Use of this device at an altitude above 4,000 into water, call equipment supplier/qualified
ft (1230 m) or outside a temperature of 50° F technician for examination and repair.
to 95° F (10° C to 35° C) or a relative humidity – NEVER drop or insert any object or liquid into
above 60% is expected to adversely affect the any opening.
flowrate and the percentage of oxygen and – For Indoor Use ONLY.
consequently the quality of therapy.

12 1195054-C
 Safety

2.3 Radio Frequency Interference concentrator Off. If the interference with the other device(s)
stops, then the concentrator is causing the interference. In
WARNING! such rare cases, interference may be reduced or corrected
Risk of Injury or Damage by one of the following measures:
To reduce the risk of injury or product damage
from interference with wireless equipment: • Reposition, relocate, or increase the separation between
– Keep concentrator at least 3.0 m (9.8 ft) away the equipment.
from wireless communication equipment such • Connect the equipment into an outlet on a circuit
as wireless home network devices, mobile different from that to which the other device(s) is
phones, cordless phones and base stations, connected.
walkie-talkies, etc. For additional information, refer to 10.2
Electromagnetic Compliance (EMC), page 39.
WARNING!
– Use of accessories and cables other than those
specified or provided by Invacare could result
in increased electromagnetic emissions or
decreased electromagnetic immunity of this
equipment and result in improper operation.

This equipment has been tested and found to comply

with EMC limits specified b y I EC/EN 6 0601-1-2 f or Type
BF equipment. These limits are determined to provide
reasonable protection against electromagnetic interference
in a typical home healthcare environment. Use of this
equipment in an environment with higher levels of
interference could affect the accuracy of the oxygen
concentration being delivered. This equipment is not
intended for use in a professional healthcare environment.
Other devices may experience interference from even
the low levels of electromagnetic emissions permitted by
the above standards. To determine if the emissions from
the concentrator are causing the interference, turn the
1195054-C 13
Invacare® Platinum® Oxygen Concentrator

3 Components F Elapsed Time Meter

G Cabinet Filter
3.1 Component Identification
Rear View

H Power Cord
I HomeFill Outlet Fitting

Accessories (Not Shown): HomeFill Home Oxygen

Compressor — IOH200AW
The HomeFill outlet fitting I is to be used only
for filling oxygen cylinders with the HomeFill Home
Oxygen Compressor. The outlet fitting does not
affect concentrator performance. Refer to the
HomeFill System user manual for connection and
A Oxygen Outlet operating instructions. When not in use, the plug
provided with the concentrator should be inserted
B Flowmeter into the outlet fitting. For more information about
C Oxygen Purity Indicator Lights/Fault and the HomeFill System, contact your Invacare dealer.
Power Indicator Lights
D Power Switch
E Circuit Breaker

14 1195054-C
 Components

3.2 Pneumatic Diagram

Fig. 3-2 Concentrator with Humidifier

Fig. 3-1 Concentrator without Humidifier

1195054-C 15
Invacare® Platinum® Oxygen Concentrator

4 Accessories
4.1 Optional Accessories
There are many different types of humidifiers, oxygen
tubing, cannulas and masks that can be used with this
device. You should contact your local home care supplier for
recommendations on which of these devices will be best for
you. They should also give you advice on the proper 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 to reduce the propagation of fire in
the accessories for the safety of the patient and others. If
a commercially available, fire-activated flow stop device is
used in the accessories setup, it should be placed as close
to the patient as possible.
• High Flow Adult Nasal Cannula 2.1 m (7 ft) - 1524236
• High Flow Humidifier - 1509582
• HomeFill Home Oxygen Compressor - IOH200AW
• Oxygen Supply Tubing 4.5 m (15 ft) - M4150
• Oxygen Supply Tubing 7.6 m (25 ft) - M4250
• Oxygen Tubing Connector - M4650
• Power Cord Assembly - 1156533

16 1195054-C
 Setup

5 Setup 1. Check for any obvious damage to the carton or its

contents. If damage is evident, notify the carrier, or
your local dealer.
5.1 Unpacking 2. Remove all loose packing from the carton.
3. Carefully remove all the components from the carton.
Unless the oxygen concentrator is to be used
IMMEDIATELY, leave concentrator in its packaging
for storage 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 to 10.1 Specifications, page 36 for storage
temperature parameters.
2. DO NOT place objects on top of repackaged concentrator.

1195054-C 17
Invacare® Platinum® Oxygen Concentrator

6 Usage WARNING!
Risk of Injury or Damage
6.1 Introduction To avoid injury or damage from airborne
pollutants and/or fumes and for optimal
Your oxygen concentrator is intended for individual use performance:
indoors. It is an electronically operated device that separates – Locate and position the concentrator in a well
oxygen from room air. It provides high concentration of ventilated space so that the air intake and the
oxygen directly to you through a nasal cannula. Clinical air exhausts are not obstructed.
studies have documented that oxygen concentrators are – NEVER block the air openings of the
therapeutically equivalent to other types of oxygen delivery concentrator or place it on a soft surface, such
systems. as a bed or couch, where the air opening may
be blocked.
Your supplier will show you how to use your oxygen – Keep the openings free from lint, hair and
concentrator. He/She should be contacted with any similar foreign items.
questions or problems regarding your oxygen concentrator. – Keep concentrator at least 30.5 cm (12 in) away
This user manual will tell you about your concentrator and from walls, draperies and furniture.
will serve as a reference as you use your concentrator. – Avoid use in presence of pollutants, smoke or
fumes, flammable anesthetics, cleaning agents
6.2 Select a Location or chemical vapors.
WARNING! – Place concentrator in a well ventilated area to
Risk of Injury avoid airborne pollutants and/or fumes.
To avoid injury during therapy: – DO NOT use in a closet.
– The oxygen concentrator MUST be placed on a
level surface for use.
– DO NOT relocate the oxygen concentrator while
in use.

18 1195054-C
 Usage

You may select a room in your house where using your 6.3.1 Setting Up the Humidifier (If Prescribed)
oxygen concentrator would be most convenient. Your
concentrator can be easily rolled from room to room on WARNING!
its casters. Risk of Injury or Damage
To avoid burns from steam or hot water,
Your oxygen concentrator will perform best when operated inhalation of water and/or water damage to the
under the conditions outlined in 10.1 Specifications, page 36. concentrator:
– DO NOT fill humidifier bottle with hot water.
Usage in environments other than those described may
Allow boiled water to cool to room temperature
result in the need for increased equipment maintenance.
before filling.
The air intake of the unit should be located in a well
– DO NOT overfill humidifier.
ventilated area to avoid airborne pollutants and/or fumes.
– Replace the humidifier cap and securely tighten.
6.3 Setting Up the Concentrator Confirm that the cap is not cross-threaded on
the humidifier bottle.
1. Plug in power cord to an electrical outlet. – DO NOT reverse the oxygen input and output
2. Connect Humidifier (if so prescribed). connections. Water from the humidifier bottle
will travel through the cannula back to the
patient if input and output connections are
reversed.
– When using tubing connections longer than
2.1 m (7 ft) in length, position the humidifier
as close to the patient as possible to allow for
maximum humidification output.

1195054-C 19
Invacare® Platinum® Oxygen Concentrator

Humidifier Bottle Humidifier Bottle without Cap 3. Insert a flathead screwdriver in the plate groove C on
with Cap the top edge of the filter access door D and gently pry
the filter access door off.

4. Pull up and remove the humidifier bottle adapter E

1. Remove cap A from bottle B. (next to inlet filter).
2. Fill humidifier bottle with boiled tap water or bottled
water to the level indicated by the manufacturer. Boil
tap water for approximately ten minutes and cool to
room temperature prior to use.
CAUTION!
Risk of Damage
– Confirm the humidifier cap is not
cross-threaded on the humidifier bottle.

WARNING!
Risk of Injury
To avoid impacting the flow of oxygen:
– Install the humidifier bottle and/or other
accessories properly.

20 1195054-C
 Usage

5. Attach the humidifier bottle adapter E to the humidifier 6. When placing the humidifier bottle in the compartment
bottle B by turning the wing nut G on the humidifier F on the concentrator, attach the humidifier
bottle counterclockwise until it is securely fastened. bottle/adapter tube H to the oxygen outlet connector
I on the concentrator.

When using tubing connections longer than 2.1

m (7 ft) in length, position the humidifier as
close to the patient as possible to allow for
maximum humidification output.

7. Connect the nasal cannula. Refer to 6.3.2

Connecting/Positioning the Nasal Cannula, page 22.
8. Replace the filter access door on the side of concentrator
by snapping it back into the plate groove.

1195054-C 21
Invacare® Platinum® Oxygen Concentrator

6.3.2 Connecting/Positioning the Nasal Cannula WARNING!

Risk of Injury or Death
DANGER! To reduce the risk of injury or death from illness:
Risk of Injury or Death – Replace the nasal cannula on a regular basis.
The cannula can cause tripping, falling, or other Check with your equipment provider or
injury if improperly positioned and secured. To physician to determine how often the cannula
avoid injury or death: should be replaced.
– The cannula MUST be routed and secured – DO NOT share cannulas between patients.
properly. Cannulas are for single patient use only.
– DO NOT position the cannula around the neck.
Ensure the patient can move freely while
wearing the cannula. CAUTION!
– Avoid positioning cannulas across areas of high Risk of Minor Injury or Discomfort
foot traffic (i.e. aisles, doorways, hallways, etc.) To ensure proper oxygen delivery:
– Ensure the cannula prongs are positioned
properly in your nose. This is critical to the
WARNING! effectiveness of the oxygen therapy.
Risk of Injury or Death – DO NOT use tubing/cannula length exceeding
To avoid choking and/or strangulation from tubing 15 m (50 ft).
entanglement: – Use crush-proof oxygen tubing.
– Keep children and pets away from nasal – Check for gas flow at the outlet of the cannula.
cannula and tubing.
– Close supervision is necessary when the nasal
cannula is used by impaired individuals or near
children and/or impaired individuals.

22 1195054-C
 Usage

Fig. 6-2 Concentrator with Humidifier

Fig. 6-1 Concentrator without Humidifier

1. Remove the cannula from its packaging. 3. Perform one of the following:
2. Place the cannula A over your ears and position the • For use with a humidifier bottle—Attach the
prongs in your nose as instructed by your health care patient’s nasal cannula supply tube B to the
provider or cannula manufacturer. humidifier bottle outlet M.
• For use without a humidifier bottle—Attach the
patient’s nasal cannula supply tube B to the
oxygen outlet connector K on the concentrator.
4. After assembly, ensure that oxygen is flowing
through the nasal cannula. Refer to6.3.3 Turning the
Concentrator On, page 24 and 6.3.4 Flowrate, page 25.
1195054-C 23
Invacare® Platinum® Oxygen Concentrator

Gas flow at the outlet of the cannula can be checked 6.3.3 Turning the Concentrator On
while the concentrator is warming up. Wave your
hand in front of the nasal prongs. You should be
able to hear and feel the flow of gas. If you do not
feel the gas , check the cannula connection for leaks.

WARNING!
Risk of Injury or Damage
Failure to properly install the humidifier bottle or
other accessories to the concentrator will impact
the flow of oxygen.
– To check for proper operation of the oxygen
concentrator and accessories, place the end 1. Press power switch A to On position.
of the nasal cannula under the surface of a
half-full cup of water, only when the oxygen is All the panel lights and the audible alarm will
flowing, and look for bubbles indicating proper come on for one second, confirming that the
operation. Wipe any excess water off the nasal indicators are functioning properly.
prongs when finished before placing on the
patient.
– If there are no bubbles, check all connections
(including humidifier bottle and other
accessories, if applicable) and repeat. Contact
your dealer or service provider immediately if
bubbles still do not appear.

24 1195054-C
 Usage

6.3.4 Flowrate 1. Turn the flowrate knob A to the setting prescribed by

your physician or therapist.
WARNING!
Risk of Minor Injury or Discomfort To properly read the flowmeter B, locate the
It is very important to select the prescribed prescribed flowrate line on the flowmeter. Next,
oxygen flow setting. This will ensure you will turn the flow knob until the ball C rises to the
receive the therapeutic amount of oxygen line. Now, center the ball on the L/min line
according to your medical condition. prescribed.
– DO NOT increase or decrease the L/min flow
setting unless a change has been prescribed by
your physician or therapist. 2. If the flowrate on the flowmeter ever falls below 0.5
– The therapeutic effectiveness of the prescribed L/min for more than about one minute, the Potential
oxygen flow setting should be periodically Obstruction Alert will be triggered. This is a rapid
reassessed. beeping of the audible alarm. Check your tubing or
– Use only the tubing and accessories that were accessories for blocked or kinked tubing or a defective
used to determine the prescribed oxygen flow humidifier bottle. After rated flow is restored to
setting. between 0.5 L/min and 0.75 L/min, the Potential
Obstruction Alert will turn off.
A Potential Obstruction Alert indicates a condition
that may be associated with a partial or complete
obstruction of oxygen output.
The use of some accessories and the HomeFill
compressor will deactivate the Potential Obstruction
Alert.

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Invacare® Platinum® Oxygen Concentrator

6.3.5 SensO2 Oxygen Purity Indicator 6.3.7 Explanation of Oxygen Purity Indicator Lights
This feature monitors the purity of oxygen generated
by the oxygen concentrator. If purity falls below factory
preset standards, indicator lights on the control panel will
illuminate.
6.3.6 Initial Startup of the Concentrator
Concentrator may be used during the initial warm-up
time (approximately 30 minutes) while waiting for
the O2 purity to reach maximum.

When the unit is turned on the yellow light will come on Indicator Explanation
O2
indicating the unit is operating and is in the initial warm-up Symbol Light
Purity
period. When the green light comes on the unit is in normal (LED)
operating mode (SYSTEM OK/O2 greater than 85%). Once
SYSTEM No action is
in normal operating mode the lights will be controlled
OKAY GREEN needed. Normal
depending on the oxygen concentration values. A O2
O2 over light for operation.
85%
Immediately call
supplier. You may
continue to use
O2 the concentrator
YELLOW
between unless instructed
B light
73% and otherwise by
(Solid)
85% your supplier.
Be certain that
backup oxygen is
nearby.

26 1195054-C
 Usage

Indicator Explanation
O2
Symbol Light
Purity
(LED)
Immediately
GREEN call supplier.
O2 light with Oxygen sensor
O2 un-
AB YELLOW is malfunctioning.
known
light You may continue
flashing to use the
concentrator.
Continuous
Audible Alarm
Sieve-GARD™
Compressor
SYSTEM
Shutdown
FAILURE
RED light
C O2 SYSTEM FAILURE.
(Solid)
below Total unit
73% shutdown.
Immediately
switch to backup
oxygen supply and
call supplier.
D — — Call supplier.

6.3.8 Elapsed Time Meter (Hour Meter)

The hour meter displays the cumulative number of hours the
unit has operated. Refer to 3.1 Component Identification,
page 14 for specific location.

1195054-C 27
Invacare® Platinum® Oxygen Concentrator

7 Maintenance DANGER!
Risk of Injury or Damage
7.1 Service Life Liquid will damage the internal components of
the concentrator. To avoid damage or injury from
The expected service life of this product is three years electrical shock:
of operation when used in accordance with the safety – Turn Off the concentrator and unplug the
instructions, maintenance intervals and correct use, stated power cord before cleaning.
in this manual. The effective service life can vary according – DO NOT allow any cleaning agent to drip inside
to frequency and intensity of use. Refer to the procedures the air inlet and outlet openings.
in the Maintenance section. – DO NOT spray or apply any cleaning agent
directly to the cabinet.
7.2 Cleaning the Cabinet – DO NOT hose down the product.
DANGER! CAUTION!
Risk of Injury or Damage Risk of Damage
Invacare oxygen concentrators are specifically Harsh chemical agents can damage the
designed to minimize routine preventive concentrator. To avoid damage:
maintenance. To prevent injury or damage: – DO NOT clean the cabinet or filter with alcohol
– Only qualified personnel should perform and alcohol based products (isopropyl alcohol),
preventive maintenance on the oxygen concentrated chlorine-based products (ethylene
concentrator. chloride), and oil-based products (Pine-Sol®,
– DO NOT remove cabinet. Lestoil®) or any other harsh chemical agents.
Only use mild liquid dish detergent (such as
Dawn®).

At a minimum, preventive maintenance MUST be

performed according to the maintenance record
guidelines. In places with high dust or soot levels,
maintenance may need to be performed more often.
Refer to 7.6 Preventive Maintenance Checklist, page
32.

28 1195054-C
 Maintenance

Periodically clean the concentrator’s cabinet as follows:

1. Use a damp cloth or sponge with a mild detergent,
such as Dawn dish washing soap, to gently clean the
exterior case.
2. Allow the concentrator to air dry or use a dry towel
before operating the concentrator.

7.3 Cleaning the Cabinet Filter

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

There are two cabinet filters located on each side

of the cabinet.

1195054-C 29
Invacare® Platinum® Oxygen Concentrator

1. Remove the filter A and clean as needed.

Environmental conditions that may require more
frequent inspection and cleaning of the filter
include, but are not limited to: high dust, air
pollutants, etc.

2. Clean the cabinet filter with a vacuum cleaner or wash

with a mild liquid dish detergent (such as Dawn) and
water. Rinse thoroughly.
3. Thoroughly dry the filter and inspect for fraying,
crumbling, tears and holes. Replace filter if any damage
is found.
4. Reinstall the cabinet filter.

30 1195054-C
 Maintenance

7.4 Humidifier Cleaning and Thermic Disinfection 1. Dispose of and replace all patient side accessories not
suitable for multiple patient use, including but not
Clean and disinfect the oxygen humidifier daily to limited to:
reduce limestone deposits and eliminate possible
bacterial contamination. Follow the instructions • Nasal Cannula and Tubing
provided by the manufacturer. If none are provided, • Mask
follow these steps: • Humidifier
2. Perform maintenance procedures described in this
1. Wash humidifier in soapy water and rinse with a manual and items on the Preventive Maintenance
solution of ten parts water and one part vinegar. Checklist.
2. Rinse thoroughly with hot water. 3. Check concentrator for possible external damage or
3. Air dry thoroughly. signs that it may require service or repair.
To limit bacterial growth, air dry the humidifier 4. Ensure concentrator functions properly and all alarms
thoroughly after cleaning when not in use. Refer to are in working order.
6.3 Setting Up the Concentrator, page 19 for use. 5. Before repackaging and distribution to new patient,
ensure packaging contents contain the concentrator,
user manual, power cord, assembly instructions and
7.5 Cleaning and Disinfection Between Patients labels.
WARNING!
Risk of Injury or Damage
To prevent injury from infection or damage to
concentrator:
– Only qualified personnel should perform
cleaning and disinfection of the oxygen
concentrator and accessories between patients.

Follow these instructions to eliminate possible

pathogen exchange between patients due to
contamination of components or accessories.
Preventive maintenance should also be performed
at this time if necessary.

1195054-C 31
Invacare® Platinum® Oxygen Concentrator

7.6 Preventive Maintenance Checklist

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 Flowrate
DURING PREVENTIVE MAINTENANCE SCHEDULE, OR BETWEEN PATIENTS
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 supplier or qualified service technician. Refer to service manual.

26,280 hours are equivalent to usage 24 hours per day, 7 days per week for 3 years.

32 1195054-C
 After Use

8 After Use 8.2 Wear and Tear

Invacare reserves the right to ask for any item back that
8.1 Recycling Information has an alleged defect in workmanship. See Warranty that
shipped with the product for specific warranty information.
This product has been supplied from an environmentally
aware manufacturer who complies with the Waste Electrical Refer to this user manual for proper preventive maintenance
and Electronic Equipment (WEEE) Directive 2012/19/EU. This schedule and use of the product.
product may contain substances that could be harmful to
the environment if disposed of in places (landfills) that are This is just a general guideline and does not include items
not appropriate according to legislation. damaged due to abuse and misuse.

Follow local governing ordinances and recycling plans Normal wear and tear items and components for this
regarding disposal of the concentrator or components product are listed below.
normally used in operation. The concentrator does not • All types of filters
generate waste or residue in operation. • All types of tubing
• DO NOT dispose of the concentrator in the normal Sieve is a porous filtering material and is considered
waste stream. a wear item. Some factors that could affect
• Any accessories not part of the concentrator MUST sieve material life include humidity, temperature,
be handled in accordance with the individual product particulates, air contaminates, air intake, vibration
marking for disposal. and other environmental conditions.
Invacare is continuously working towards ensuring that the
company’s impact on the environment, locally and globally,
is reduced to a minimum. We comply with the current
environmental legislation (e.g. WEEE and RoHS directives).
We only use REACH compliant materials and components.

1195054-C 33
Invacare® Platinum® Oxygen Concentrator

9 Troubleshooting
9.1 Troubleshooting
SYMPTOM PROBABLE CAUSE SOLUTION
Alarm: Main Power Loss:
No lights illuminated or lights 1. Power cord not plugged in. 1. Insert plug into outlet.
flashing intermittently. 2. No power at outlet. 2. Inspect house circuit breakers or fuses. If problem
3. Tripped circuit breaker. recurs, use a different outlet.
Short Beeps, long pause 4. Unit overheated, tripping 3. Push/reset circuit breaker. If problem recurs, call
Concentrator not operating, internal thermal protector. service supplier.
power switch On. 4. Turn power switch off and allow unit to cool. Do
one or both of the following:
Beep...Beep...
a. Remove and clean cabinet filters.
b. Move oxygen concentrator at least 30.5 cm (12
in) away from walls, draperies or furniture.
Turn power switch on. If problem recurs, call service
provider.
Alarm: System Failure:
RED light illuminated. 1. Unit overheating due to 1. Do one or both of the following:
blocked air intake.
Continuous a. Remove and clean cabinet filters.
2. Insufficient power at outlet.
b. Move oxygen concentrator at least 30.5 cm (12
Concentrator not operating, 3. Internal repairs required.
in) away from walls, draperies or furniture.
power switch On.
2. DO NOT use extension cords. Move to another
Beep... electrical outlet or circuit.
3. Call service supplier.

34 1195054-C
 Troubleshooting

SYMPTOM PROBABLE CAUSE SOLUTION

Alarm: Potential Obstruction Alert
GREEN light illuminated. 1. Possible internal obstruction 1. Inspect for kinks or blockages. Correct, clean or
in the oxygen path. Kinked replace item. Once corrected, turn power Off for 60
Rapid or blocked tubing, cannula or seconds and then turn power back On.
Beep...Beep... humidifier. 2. Reset flowmeter to prescribed flowrate.
2. Flowmeter set at 0.5 L/min or
Beep...Beep less.
Alarm: System Failure:
YELLOW light Illuminated. 1. Low oxygen purity. 1. Clean or Replace filters.
2. Kinked or blocked tubing, 2. Inspect for kinks or blockages. Correct, clean or
Short beeps, long pause cannula or humidifier. replace item. Once corrected, turn power Off for 60
Beep...........Beep............. 3. Flowmeter set at 0.5 L/min or seconds and then turn power back On.
less. 3. Check flowmeter is set to 1.0 L/min or more. Refer
to 10.1 Specifications, page 36.
GREEN light with YELLOW 1. Internal repairs required. 1. Call service supplier.
Light Flashing.

1195054-C 35
Invacare® Platinum® Oxygen Concentrator

10 Technical Data
10.1 Specifications
Electrical Requirements: 230 VAC +10, -15% (253 VAC/195.5 VAC), 50 Hz
Rated Current Input: 2.3 A
Sound Pressure Level: < 50 dBA weighted for 3 L/min flow
< 50 dBA weighted for 9 L/min flow
Sound Power Level: < 50 dBA weighted for 9 L/min flow
Altitude: Up to 1230 m (4,000 ft) above sea level without degradation of concentration levels.
Atmospheric Pressure Range: 101.33 kPa – 88.0 kPa
Oxygen Output Concentration 92% minimum at 1 to 2 L/min
Levels: 93% minimum at 3 to 7 L/min
91% minimum at 8 L/min
87% minimum at 9 L/min
Concentration levels achieved after initial warm-up period (approximately 30
minutes)

Maximum Outlet Pressure: 62.0 kPa ± 3.45 kPa (9 psi ± 0.5 psi)
Flow Range: 1 L to 9 L/min. Flowrates less than 1 L/min are not recommended.
Potential Obstruction Alert: The concentrator detects a condition that may indicate a potential obstruction of the
output oxygen. Rapid audible beeping alert (this alert is deactivated when accessories
are connected) may be associated with flow setting of 0.5 L/min or less.
Power Consumption: 460 W Typical

36 1195054-C
 Technical Data

Pressure Relief Mechanism 241 kPa ± 34.5 kPa (35 psi ± 5 psi)
Operational at:
Change in maximum recommended 0.7 L/min
flow when back pressure of 7 kPa
is applied:
Filters: Cabinet (2), Outlet HEPA and Compressor Inlet
Safety System: Current overload or line surge shutdown.
High temperature compressor shutdown.
Internal High Temperature 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: 46.7 cm ± 1 cm (18 3/8 in ± 3/8 in)
Height: 67.0 cm ± 1 cm (26 3/8 in ± 3/8 in)
Depth: 36.5 cm ± 1 cm (14 3/8 in ± 3/8 in)
Weight: 24.0 kg ± 1 kg (53 lb ± 2 lb)
Shipping Weight: 27.2 kg ± 1 kg (60 lb ± 2 lb)
Operating Ambient Temperature 10°C to 35°C (50°F to 95°F) at up to 60% relative humidity
and Humidity:
Cabinet: Impact Resistant flame-retardant plastic cabinet that conforms to UL 94 V-0
No AP/APG: Not suitable for use in the presence of a flammable anaesthetic mixture.

1195054-C 37
Invacare® Platinum® Oxygen Concentrator

Standards and Regulatory Listing: Certified complying with:

IEC/EN 60601-1
IEC/EN 60601-1-2
IEC/EN 60601-1-6
IEC/EN 60601-1-11
ISO 80601-2-69
CE marked model: IRC9LXO2AWQ
Electrical: No extension cords.
Placement: No closer than 30.5 cm (12 in) from any wall, furniture, draperies or similar 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).
Environment: Smoke and soot-free
Tubing: Recommended use up to 15.2 m (50 ft) high flow tubing with high flow cannula at
all flow rates.
Time of Operation: Up to 24 hours per day
Recommended Storage and Shipping -29°C to 65°C (-20°F to 150°F) at up to 95% relative humidity
Temperature:

Measurement uncertainty is included in the device specification. All conditions at STPD (standard temperature and
pressure dry).

38 1195054-C
 Technical Data

10.2 Electromagnetic Compliance (EMC)

Guidance and manufacturer´s declaration—electromagnetic emission
The Device is intended for use in the electromagnetic environment specified below. The customer or the user of the Device
should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance
The Device uses RF energy only for its internal function. Therefore, its RF emissions
RF emissions
Group I are very low and are not likely to cause any interference in nearby electronic
CISPR 11
equipment.
RF emissions
Class B
CISPR 11
Harmonic
The Device is suitable for use in all establishments including domestic
emissions Class A
establishments and those directly connected to the public low-voltage power
IEC 61000-3-2
supply network that supplies buildings used for domestic purposes.
Voltage fluctuations
/ flicker emissions Complies
IEC 61000-3-3

Guidance and manufacturer´s declaration—electromagnetic immunity

The Device is intended for use in the electromagnetic environment specified below. The customer or the user of the Device
should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment – guidance
Electrostatic Floors should be wood, concrete or ceramic tile.
± 2, 4, 8 kV contact ± 2, 4, 8 kV contact
discharge (ESD) If floors are covered with synthetic material, the
± 2, 4, 8, 15 kV air ± 2, 4, 8, 15 kV air relative humidity should be at least 30%.
IEC 61000-4-2

1195054-C 39
Invacare® Platinum® Oxygen Concentrator

Electrical Fast
transient / burst Mains power quality should be that of a typical
± 2 kV mains, 100kHz ± 2 kV mains, 100kHz
commercial or hospital environment.
IEC 61000-4-4
Surge ± 1 kV line(s) to line(s) ± 1 kV line(s) to line(s) Mains power quality should be that of a typical
IEC 61000-4-5 ± 2 kV line(s) to ground ± 2 kV line(s) to ground commercial or hospital environment.

0% UT ; 1/2 cycle @ 0, 0% UT ; 1/2 cycle @ 0,

45, 90, 135, 180, 225, 45, 90, 135, 180, 225, Mains power quality should be that of a typical
270, and 315 270, and 315 commercial or hospital environment. If the user
of the Device requires continued operation during
Voltage dips and and power mains interruptions, it is recommended that
0% UT ; 1 cycle 0% UT ; 1 cycle the Device be powered from an un-interruptible
IEC 61000-4-11 power supply or a battery.
and and
UT is the a. c. mains voltage prior to application
70% UT ; 25/30 cycles 70% UT ; 25/30 cycles of the test level.
Single phase: at 0° Single phase: at 0°
Mains power quality should be that of a typical
commercial or hospital environment. If the user
of the Device requires continued operation during
Voltage
power mains interruptions, it is recommended that
Interruptions 0% UT ; 250/300 cycle 0% UT ; 250/300 cycle the Device be powered from an un-interruptible
IEC 61000-4-11 power supply or a battery.
UT is the a. c. mains voltage prior to application
of the test level.
Power frequency
(50/60 Hz) Power frequency magnetic fields should be at
magnetic field 30 A/m, 50/60 Hz 30 A/m, 50/60 Hz levels characteristic of a typical location in a typical
commercial or hospital environment.
IEC 61000-4-8
40 1195054-C
 Technical Data

Portable and mobile RF communications equipment

should be used no closer to any part of the
Device including cables, than the recommended
separation distance calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance:
Conducted RF
3 Vrms, 6 Vrms 3 Vrms, 6 Vrms d = 1.2√P 150 kHz to 80 MHz
IEC 61000-4-6

Radiated RF 10 V/m 10 V/m d = 0.35√P 80 MHz to 800 MHz

IEC 61000-4-3 d = 0.7√P 800 MHz to 2,5 GHz
where P is the maximum output power rating
of the transmitter in watts (W) according to
the transmitter manufacturer and d is the
recommended separation distance in metres (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey,a
should be less than the compliance level in each
frequency range.b
Interference may occur in the vicinity of equipment
marked with the following symbol:

a Field strengths from fixed t ransmitters, s uch a s b ase s tations f or r adio ( cellular/cordless) t elephones a nd l and m obile radios,
amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess
the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the
1195054-C 41
Invacare® Platinum® Oxygen Concentrator

measured field strength in the location in which the Device is used exceeds the applicable RF compliance level above, the Device
should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary,
such as reorienting or relocating the Device.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than [V1] V/m.
At 80 MHz and 800 MHz, the higher frequency range applies.
Recommended separation distances between portable and mobile RF communications equipment and the Device
The Device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The
customer or the user of the Device can help prevent electromagnetic interference by maintaining a minimum distance between
portable and mobile RF communications equipment (transmitters) and the Device as recommended below, according to the
maximum output power of the communications equipment
Separation distance according to frequency of transmitter [m]
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
Rated maximum output
of transmitter [W] d = 1.2√P d = 0.35√P d = 0.7√P
0.01 0.12 0.04 0.07
0.1 0.37 0.11 0.22
1 1.17 0.35 0.70
10 3.69 1.11 2.21
100 11.67 3.50 7.00

42 1195054-C
 Technical Data

For transmitters rated at a maximum output power not listed above the recommended separation, distance d in meters (m)
can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power
rating of the transmitter in watts (W) according to the transmitter manufacturer.
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.

1195054-C 43
Invacare® Platinum® Oxygen Concentrator

11 Warranty
11.1 Customer Service and Warranty Information
Terms and conditions of the warranty are part of the general terms and conditions particular to the individual countries in
which this product is sold.
Belgium & Luxemburg: Invacare nv • Autobaan 22, B-8210 Loppem • Tel: (32) (0) 50 83 10 10 •
marketingbelgium@invacare.com • www.invacare.be
Danmark: Invacare A/S • Sdr. Ringvej 37, DK-2605 Brøndby • Tel: (45) (0)36 90 00 00 • denmark@invacare.com
• www.invacare.dk
Deutschland: Invacare GmbH • Am Achener Hof 8, D-88316 Isny • Tel: (49) 7562 700 0 • kontakt@invacare.com •
www.invacare.de
Eastern Europe, Middle Invacare EU Export • Route de St Roch, F-37230 Fondettes, France • Tel: (33) (0)2 47 62 69 80 •
East & CIS: serviceclient_export@invacare.com • www.invacare.eu.com
Invacare SA • Avenida Del Oeste n.50-1o-1a, Valencia-46001 • Tel: (34) 972 493 214 •
España: contactsp@invacare.com • www.invacare.es
Invacare Poirier SAS • Route de St Roch, F-37230 Fondettes • Tel: (33) (0)2 47 62 64 66 •
France: contactfr@invacare.com • www.invacare.fr
Ireland: Invacare Ireland Ltd • Unit 5 Seatown Business Campus, Seatown Road, Swords, County Dublin,
EirCode: K67 K271-Ireland • Tel: (353) 1 810 7084 • ordersireland@invacare.com • www.invacare.ie
Italia: Invacare Mecc San s.r.l. • Via dei Pini 62, I-36016 Thiene (VI) • Tel: (39) 0445 38 00 59 •
servizioclienti@invacare.com • www.invacare.it
Nederland: Invacare BV • Galvanistraat 14–3, NL–6716 AE Ede • Tel: (31) (0)318 695 757 •
nederland@invacare.com • www.invacare.nl
Norge: Invacare AS • Brynsveien 16, Postboks 6230, Etterstad, N-0603 Oslo • Tel: (47) (0)22 57 95 00 •
norway@invacare.com • island@invacare.com • www.invacare.no
Österreich: Invacare Austria GmbH • Herzog-Odilo-Straße 101, A-5310 Mondsee • Tel: (43) 6232 5535 0 •
info@invacare-austria.com • www.invacare.at
Portugal: Invacare Lda • Rua Estrada Velha, 949, P-4465-784 Leça do Balio • Tel: (351) (0)225 193 360 •
portugal@invacare.com • www.invacare.pt
Sverige: Invacare AB • Fagerstagatan 9, S-163 53 Spånga • Tel: (46) (0)8 761 70 90 • sweden@invacare.com •
www.invacare.se
44 1195054-C
 Warranty

Suomi: Camp Mobility • Patamäenkatu 5, 33900 Tampere • Tel: 09-35076310 •

info@campmobility.fi • www.campmobility.fi
Schweiz/Suisse/Svizzera: Invacare AG • Benkenstrasse 260, CH-4108 Witterswil • Tel: (41) (0)61 487 70 80 •
switzerland@invacare.com • www.invacare.ch
United Kingdom: Invacare Limited • Pencoed Technology Park, Pencoed, Bridgend CF35 5AQ • Tel: (44) (0) 1656 776200
• UK@invacare.com • www.invacare.co.uk
Australia: Invacare Australia Pty Ltd • Unit 18/12 Stanton Road, Seven Hills, NSW 2147 • Tel: 1800 460 460 •
orders@invacare.com.au • www.invacare.com.au
New Zealand: Invacare New Zealand • 4 Westfield Place, Mt Wellington 1060 • Tel: 0800 468 222 •
sales@invacare.co.nz • www.invacare.co.nz
Thailand: Invacare (Thailand) Ltd • 07-120, 88 The Parq Building, 7th Floor, Ratchadaphisek Road, Klongtoey Sub-
district, Klongtoey District, Bangkok 10110 • Tel: 66 2 821 5515

1195054-C 45
Notes
Notes
Invacare Corporation
USA Manufacturer
One Invacare Way Invacare Corporation
Elyria, Ohio 44035 One Invacare Way
United States Elyria, Ohio 44035
Tel: 440–329–6000 United States
Tel: 800–333–6900
Technical Services
Tel: 440–329–6593
Tel: 800–832–4707
www.invacare.com
EU Representative
Invacare GmbH
Am Achener Hof 8
88316 Isny
Germany

1195054-C 2022-07-07
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