inogen GS-100 Oxygen Concentrator User Manual

inogen GS-100 Oxygen Concentrator

Glossary of Symbols

Symbol Key

WARNING

• A warning indicates that the personal safety of the patient may be involved. Disregarding a warning could result in significant injury

CAUTION

A caution indicates that a precaution or service procedure must be followed. Disregarding a caution could lead to a minor injury or damage to equipment

• On/Off (Power)
• Flow setting indicator
• Blue Indicator Light
• General alarm indicator light
• Follow instructions for use
• Type BF Applied Part
• Class II Equipment
• No Open Flames
• No Smoking
• No Oil or Grease
• Do Not Disassemble
• Electrical Safety Agency Certificate
• Magnetic Resonance (MR) safe
• Medical Device
• U.S. Federal Regulation Restricts this device to sale by order of a physician. May also be applicable in other countries
• Do not dispose of in the unsorted municipal waste
• AC Power
• Keep Dry
• Enclosure Ingress Protection against solid objects of 12.5mm minimum diameter and vertically falling drops of water
• Manufacturer
• Complies with applicable EU directives including medical devices directive

As Packaged (Per Box)

• Authorized representative in the European Community
• Fragile
• Humidity
• Temperature
• This Side

Warnings, Cautions and Contraindications

Contraindications

• This equipment is to be used as an oxygen supplement and is NOT INTENDED to be life-supporting or life-sustaining.

Warnings

• The device produces concentrated oxygen gas which accelerates combustion. DO NOT USE THE DEVICE WHEN SMOKING OR NEAR OPEN FLAME, MATCHES, PETROLEUM, OIL, GREASE, SOLVENTS, RADIANT HEATERS, AEROSOLS etc. Use only water-based lotions or salves that are concentrated oxygen compatible during oxygen therapy.
• Concentrated oxygen makes it easier for a fire to start and spread. Do not leave the nasal cannula on upholstery or other fabric such as bedding or personal clothing if the oxygen concentrator is turned on but not in use.
• Concentrated oxygen will make the materials flammable. Turn off the oxygen concentrator when not in use.
• Do not use the oxygen concentrator in the presence of pollutants, smoke or fumes, flammable anesthetics, cleaning agents or other chemical vapors. This may internally contaminate the oxygen concentrator and degrade its performance.
• Do not use the oxygen concentrator if either the plug or the power cord is damaged to prevent accidental electrical shock.
• Do not submerge the oxygen concentrator in liquids, expose to liquids, or otherwise allow liquids to enter into the case, this may lead to electrical shock and/or damage. If the oxygen concentrator is exposed to liquids turn it off and unplug from the electrical outlet before attempting to clean and dry the liquid spill.
• When using a compatible humidifier do not refill the humidifier while attached to the oxygen concentrator. Remove the humidifier from the oxygen concentrator prior to refilling to prevent accidental spills on the concentrator and prevent electrical shock hazards.
• Do not use cleaning agents other than those specified in this manual. Always unplug the oxygen concentrator before performing any cleaning. Do not use alcohol, isopropyl alcohol, ethylene chloride, or petroleum-based cleaners.
• This may impair the proper function and/or increase the risk of fire and burns.
• Do not disassemble the oxygen concentrator or attempt any maintenance other than the tasks described in this user manual; disassembly creates a hazard of electrical shock and will void the warranty. Servicing of the concentrator is to be performed by qualified and trained personnel only.
• Do not use any columns other than those specified in this user manual. The use of non-specified columns may create a safety hazard and/or impair equipment performance and will void the warranty.
• To avoid the danger of choking and strangulation hazards, keep tubing away from children and pets.
• If you begin to feel ill or are experiencing discomfort while using the oxygen concentrator, consult your healthcare provider immediately.

Cautions

• USA Federal law restricts this device to sale or rental by or on the order of a physician, or any other practitioner licensed by the State in which he/ she practices to use or order the use of this device; may also be applicable in other countries. Under certain circumstances, the use of non-prescribed oxygen therapy can be hazardous.
• Availability of an alternate source of oxygen is recommended in case of power outage or mechanical failure. Consult your equipment provider for type of back-up system recommended.
• Additional monitoring or attention may be required for patients using this device who are unable to hear or see alarms or communicate discomfort. If the patient shows any signs of discomfort, a physician should be consulted immediately.
• Accessories not specified for use with the oxygen concentrator may impair performance. Always use accessories according to the manufacturer’s instructions.
• Nasal cannula should be rated 5 liters per minute to ensure proper patient usage and oxygen delivery.
• Replace the nasal cannula on a regular basis. Check with your equipment provider or health care professional to determine how often the cannula should be replaced.
• It is recommended the oxygen concentrator accessory tubing and cannula include a means to reduce the propagation of fire.
• Do not operate the concentrator without the intake filter and particle filter in place. Particles drawn into the oxygen concentrator may damage the equipment.
• Refer to the environmental range specifications for proper storage and use conditions. Temperatures in excess of the indicated range may cause device malfunction.
• Do not obstruct air intake or exhaust when operating the oxygen concentrator. Blockage of air circulation or proximity to a heat source may lead to internal heat buildup and shutdown or damage. Always maintain a minimum of six inches of clearance.
• Do not place anything in the power supply port other than the supplied wall cord. Avoid the use of electrical extension cords with the concentrator. If an extension cord must be used, use an extension cord that has an
• Underwriters Laboratory (UL) Mark and a minimum wire thickness of 18 gauge. Do not connect any other device to the same extension cord.
• Do not sit or stand on the concentrator, doing so can be hazardous.
• In order to ensure a safe installation and operation of the Inogen At Home Oxygen Concentrator Model GS-100, read and understand this entire manual before using the device.
• The Inogen At Home Oxygen Concentrator has a 5 year expected life except
• 1 year expected life for user serviceable sieve bed columns.

Indications for Use

The Inogen At Home Oxygen Concentrator is used on a prescriptive basis by patients requiring supplemental oxygen. It supplies a high concentration of oxygen and is used with a nasal cannula to channel oxygen from the concentrator to the patient. The Inogen At Home Oxygen Concentrator may be used in a home or institution.

User Interfaces, Controls and Serviceable Items

User Interfaces

• General Caution Indicator Light (Low, Medium Priority Alarm)
• A yellow light indicates either a change in operating status or a condition that may need a response. A flashing light is a higher priority than non-flashing.

Blue Indicator Light (Change Column Soon)

• Column maintenance is required within 30 days.
• Contact your equipment provider to arrange service.

User Interfaces

• Audible Indicators
• An audible alarm (beep) indicates either a change in operating status or a condition that may need a response (alarm). More frequent beeps indicate higher priority conditions.

Flow Setting Indicator

• A green indicator light indicates the selected flow setting.

User Controls

• ON / OFF Button
• Press once to turn “ON”; Press and hold for one second to turn “OFF”.

Flow Setting Control Buttons

• Use the – or + flow setting control buttons to select the setting as shown on the display. There are five settings, from 1 to 5.

Serviceable Items

• Particle Filter
• The filter must be in place at the intake end of the concentrator during operation.

Air Inlet Filter

• The filter must be in place at the top of the concentrator during operation.

Cannula Nozzle Fitting

• The nasal cannula connects to this nozzle for the output of oxygen.

Nasal Cannula

• Nasal cannulas should be replaced on a regular basis, consult with your physician or equipment provider, or cannula manufacturer’s instructions.

Operating Instructions

1. Place the concentrator in a well-ventilated location; air intake and exhaust must have clear access. Ensure that the concentrator is at least 6 inches (15 cm.) away from walls, furniture and curtains that could impede adequate airflow to the device.

2. Ensure the particle filter is in place.

3. Ensure intake filter is in place.

4. Follow instructions A or B below:
   A. If you are not using a humidifier bottle, connect your nasal cannula tubing to the nozzle fitting. The nozzle fitting is located on the top of the concentrator. See illustrations 4A1 and 4A2.
   B. If you are using a humidifier bottle, follow the manufacturer’s instructions. Place the humidifier bottle in the designated holder. See illustrations 4B1 and 4B2.

5.  Attach the power cord to the back of the concentrator and plug the other end into an electrical outlet. Do not position the concentrator so that it is difficult to disconnect the power cord. Turn on the concentrator by pressing the ON/OFF button . See illustration 5. A single short beep will sound and all indicator lights will illuminate for a few seconds .

6. Use the or buttons to adjust the device to the prescribed setting. There are five flow settings, from 1 liter per minute to 5 liters per minute. The current setting can be viewed on the display. The green LED will illuminate once the set flow rate of oxygen is achieved. You may begin breathing from the device; the required oxygen concentration is normally reached within five minutes after the device is powered on.

7. Ensure that the tubing is not kinked or pinched in any way and that oxygen is flowing through the nasal cannula. If oxygen is not flowing, the green LED will not be illuminated. Refer to the troubleshooting guide section of this manual.

8. Adjust the nasal cannula so that it is properly aligned on your face or as directed by your healthcare provider.

9. Turn off the concentrator by pressing the ON/OFF button . Turn off the concentrator when not in use.

Audible and Visual Indicators

The concentrator has an audible alarm and three visual indicators (green, yellow and blue).

Notifications

• The concentrator monitors various parameters during operation and utilizes an intelligent alarm system to indicate a malfunction of the concentrator.
• Mathematical algorithms and time delays are used to reduce the probability of false alarms while still ensuring proper notification of an alarm condition
• If multiple alarm conditions are detected, the highest priority alarm will be displayed.
• To insure that audible notifications may be heard, the operators position must be determined to suit the surrounding noise level.
• Note that failure to respond to the cause of an alarm condition for low, medium and high priority alarms potentially will result in discomfort or reversible minor injury only and develop within a period of time sufficient to switch to a backup source of oxygen.
• The following notification messages are accompanied by an audible and/or visual indicator.

setting from 1-5 liters per minute
Flow rate indicator| Flow status indicator is green
Blue Indicator Light| Column maintenance is required within 30 days. Contact your equipment provider to arrange service.

Low Priority Alarms

The following low priority alarm messages are accompanied by a double beep and a solid yellow light.

Medium Priority Alarms
The following medium priority alarm messages are accompanied by a triple beep, repeated every 25 seconds, and a flashing yellow light.

High Priority Alarms
The following high priority alarm messages are accompanied by a five beep pattern, repeated every 10 seconds and a flashing yellow light warning indicating immediate response by the operator is required.

NOTE When power is lost during operation, the buzzer will alarm continuously.

Troubleshooting

Contact your home care provider if you need assistance with the device.

Any problem accompanied by information on concentrator display, visual and/or audible indicators| Refer to Chapter 4| Refer to Chapter 4
Concentrator does not power on when On/Off button is pressed| Power cord is not connected properly| Check power cord for proper connection
Malfunction| Contact your equipment provider
No oxygen| Concentrator is not powered on| Press On/Off button to power concentrator
Cannula is not connected properly or is kinked or obstructed| Check cannula and its connection
The oxygen tubing or cannula is faulty| Inspect and replace the items if necessary

Cleaning, Care and Maintenance

Cleaning and Care

• Periodically you may clean the outside case using a cloth dampened with a mild liquid detergent (such as Dawn™) and water.
• Follow manufacturer’s instructions on cleaning and care of concentrator accessories; clean or replace these accessories according to your healthcare provider or respective manufacturer’s instructions for use.

Filter Cleaning and Replacement
The particle filter must be cleaned weekly to ensure the ease of air flow. Remove filter from the side of the device.

• Clean the particle filter with a mild liquid detergent (such as DawnTM) and water; rinse in water and dry before reuse. Ensure the filter is completely dry before reinstalling into the concentrator.

Air Inlet Filter

• Replace when filter is dirty according to visual indicator.
• The air inlet filter may be replaced by the equipment provider or by the user.

Output Filter

• The output filter is intended to protect the user from inhalation of small particles in the product gas flow. The device includes an output filter conveniently located behind the removable cannula nozzle fitting. Inogen requires that this filter be replaced between patients.
• The output filter may be replaced by the equipment provider or by the user.

Routine Maintenance

• No special maintenance, other than weekly particle filter cleaning, needs to be carried out by the user.

Replacement Parts

• Contact your home care provider if you have any questions about equipment. Use only the following replacement parts:
• Inogen At Home Particle Filter (RP-400)
• Inogen At Home Output Filter Replacement Kit (RP-107)
• Inogen At Home Air Inlet Filter (RP-401)
• Inogen At Home Column Pair (RP-402)
• AC Power Cord (RP-109)

Recommended Accessories

• Humidifier Connector Tube (Salter Labs #S0-676)
• Humidifier Bottle (Salter Labs #7600)
• Nasal Cannula (Salter Labs #16SOFT)

Service

• The concentrator is specifically designed to minimize routine preventative maintenance.
• For assistance, if needed, in setting up, using, maintaining, or reporting unexpected operation or events, contact your equipment provider, or the manufacturer.

Column Change Procedure
There are two columns (metal tubes) on the concentrator located behind the particle filter. These two columns will be removed and replaced when service is required. Ensure adequate time to complete all steps without disruption is alloted when performing this maintenance.

1. Turn off the concentrator by pressing the power button to shut down the device.
2. Unplug the concentrator from the electrical outlet.
3. Lay down the concentrator on its side.
4. Press the two latch buttons on the sides of the device to remove the cover from the bottom of the concentrator in order to access the two columns.
5. Press the latch button with thumb or finger and pull the column out of the concentrator using the pull ring attached to the bottom of the column cap.
6. Remove the column completely from the concentrator.
7. Repeat steps 5-6 to remove the other column. Installation of the new columns (metal tubes):
8. Remove the upper and lower dust caps from each column. There should be a total of two dust caps removed from each column. Make sure there is no dust or debris where the dust caps were located.
9. Insert the new column into the concentrator . Do not leave the column exposed after the dust caps are removed; it should be inserted into the concentrator as soon as the dust caps have been removed, to minimize environmental exposure.
10. The spring loaded latch button should fully return to the closed position when the column is completely inserted.
11. Repeat steps 9-10 to install the other column.
12. Replace the lower cover and return the concentrator to its upright position.
13. Connect the power supply cord from the concentrator and plug into an electrical outlet. Do Not Power On the concentrator.
14. Press and hold the plus button for ten seconds. Flow indicators 1, 3 & 5 will be illuminated and column will be reset. Release the plus button.
15. Press the power button to turn on the concentrator and use normally.

NOTE Column change instructions are only to be used when maintenance is required. Columns should only be removed during this maintenance procedure.

Storage
When not in use, store indoors away from excessive moisture and temperatures. Storage conditions outside of range specified may result in damage and device malfunction.
Disposal of Equipment and Accessories
Follow your local governing ordinances for disposal and recycling of the concentrator and accessories.

Specifications, Inogen At Home, Model GS-100

15 to 95%, non-condensing

Altitude: 0 to 10,000 ft (0 to 3048 m)

Environmental Ranges for Shipping & Storage:| Temperature: -13 to 158°F (-25 to 70˚C) Humidity: 0 to 93% non-condensing

Altitude: n/a

Maximum Outlet Pressure:| 19.6-40.6 psia

(135-280 KPa Absolute)@ 20˚C

Flow Control Settings:| 5 Settings: 1 to 5 liters per minute

Standards Compliance

• This device is designed to conform to the following standards:
• EN ISO 8359:2012, Oxygen Concentrators for Medical Use – Safety Requirements (ISO 8359:1996, Second edition, Amendment 1)
• ASTM F 1464:2005, Oxygen Concentrators for Domiciliary Use
• IEC 60601-1:Edition 3.1: 2012, Medical Electrical Equipment
• Part 1: General requirements for basic safety and essential performance

Classification

• IEC Class II Equipment
• Type BF Applied Part
• IP21 Enclosure Ingress Protection against solid objects of 12.5mm minimum diameter and vertically falling drops of water
• Not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide
• Continuous Operation

Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
The Concentrator is intended for use in the electromagnetic environment specified below. The user of the Concentrator should make sure it is used in such an environment.

Immunity Test| IEC 60601

Test Level

| Compliance Level| Electromagnetic Environment – Guidance
---|---|---|---

Conducted RF IEC 61000-4-6

Radiated RF IEC 61000-4-3

|

3 Vrms

150 kHz

to 80 MHz

3V/m

80 MHz

to 2.5 GHz

|

3 Vrms 3V/m

| 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:

d=1.2√P 150 kHz to 80 MHz

d=1.2√P 80 MHz to 800 MHz

d=2.3√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 meters (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 rangeb.

Interference may occur in the vicinity of equipment marked with the following symbol:

Electrostatic discharge (ESD)

IEC 61000-4-2

| ± 6 kV contact

± 8 kV air

| ± 6 kV contact

± 8 kV air

| Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30 %.
Electrical fast transient/burst

EC 61000-4-4

| ± 2 kV for power supply lines

± 1 kV for input/output lines

| ± 2 kV for power supply lines

± 1 kV for input/output lines

| Mains power quality should be that of a typical commercial or hospital environment.
Surge

IEC 61000-4-5

| ± 1 kV line(s) to line(s)

± 2 kV line(s) to earth

| ± 1 kV line(s) to line(s)

± 2 kV line(s) to earth

| Mains power quality should be that of a typical commercial or hospital environment.
Voltage dips, short

interruptions and voltage variations on power supply input lines

IEC 61000-4-11

| <5% U T (>95%

dip in U T) for

0.5 cycle

40% U T (60%

dip in U T) for 5 cycles

70% U T (30%

dip in U T) for 25 cycles

<5% U T (>95%

dip in U T) for 5 sec

| <5% U T (>95%

dip in U T) for

0.5 cycle

40% U T (60%

dip in U T) for 5 cycles

70% U T (30%

dip in U T) for 25 cycles

<5% U T (>95%

dip in U T) for 5 sec

| Mains power quality should be that of a typical commercial or hospital environment. If the user of the [ME EQUIPMENT or

ME SYSTEM] requires continued operation during power mains interruptions, it is recommended that the

[ME EQUIPMENT or ME SYSTEM] be powered from an uninterrupted power supply or a battery.
Power frequency (50/60 Hz)

magnetic field

IEC 61000-4-8

| 3 A/m| 3 A/m| Power frequency magnetic fields should be at levels characteristic of a typical location in a typical hospital or home environment.

NOTE At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.
NOTE UT is the a.c. main voltage prior to application of the test level.

• Field strength from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile 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 measured field strength in the location in which the concentrator is used exceeds the applicable RF compliance level above, the concentrator should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the device.
• Over the frequency range 150 kHz to 80 MHz, the field strengths should be less than 3V/m.

Recommended Separation Distances between Portable and Mobile RF Communications Equipment and This Device

This concentrator is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The user of the concentrator can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and this concentrator as recommended below, according to the maximum output power of the communications equipment.

Rated Maximum Power Output of Transmitter (W)| Separation Distance According to Frequency of Transmitter (M)
---|---
 | 150 kHz to 80 MHz

d=1.2√P

| 80 MHz to 800 MHz

d=1.2√P

| 800 MHz to 2.5 GHz

d=2.3√P

0.01| 0.12| 0.12| 0.23
0.1| 0.38| 0.38| 0.73
1| 1.2| 1.2| 2.3
10| 3.8| 3.8| 7.3
100| 12| 12| 23

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.

NOTE At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE The guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

Guidance and Manufacturer’s Declaration – Electromagnetic Emissions
The concentrator is intended for use in the electromagnetic environment specified below. The user of the concentrator should assure that it is used in such an environment.

Emissions Test| Compliance| Electromagnetic Environment – Guidance
---|---|---
RF emissions CISPR 11| Group 1| The concentrator uses RF energy only for its internal function. Therefore its RF emissions are very low and not likely to cause any interference in nearby equipment.
RF emissions

CISPR 11

| Class B| The concentrator is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.
Harmonic Emissions

IEC 61000-3-2

| Class A
Voltage fluctuations

/ flicker emissions IEC 61000-3-3

| Complies

Inogen, Inc.

• 301 Coromar Drive,
• Goleta, CA 93117
• Toll Free: 877-466-4362
• +1-805-562-0515 (Outside the USA)
• E-mail: info@inogen.net.
• www.inogen.com.

Europe Authorized Representative EMERGO EUROPE Prinsessegracht 20 2514 AP, The Hague The Netherlands.

UK Responsible Person

• Emergo Consulting (UK) Limited
• c/o Cr360 – UL International
• Compass House, Vision Park Histon
• Cambridge CB24 9BZ
• United Kingdom

Independent Living Specialists

• Unit 1 / 12 Mars Road
• Lane Cove West NSW 2066
• Tel: 02 9427 4995

BOC Limited

• 10 Julius Avenue, North Ryde,
• NSW 2113,
• Australia
• Tel: 1800 050 999
• 988 Great South Road,
• Penrose Auckland,
• New Zealand
• Tel: 0800 699 2273

Air Liquide Healthcare

• Level 4, Suite 3-4 247 Coward Street
• Mascot NSW 2020
• Tel: 1300 360 202

References

• Inogen Portable Oxygen Concentrators | Oxygen Therapy

Read User Manual Online (PDF format)

Download This Manual (PDF format)

Download this manual  >>