Drive DeVilbiss iGo 2 Portable Oxygen Concentrator

Service Manual

MODEL 125D
MODEL 125K
MODEL 125A

DANGER-NO SMOKING

CAUTION
Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.

Assembled in USA
 TABL E O F C O N TEN TS

GENERAL INFORMATION SERVICING AND COMPONENT REPLACEMENT

Symbol Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Cover. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Important Safeguards. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 Control Panel Label . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Operating Principle. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 Oxygen Outlet Port and Final Bacteria Filter . . . . . . . . . . . . . . . 18
Technical Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 Sieve Beds. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Healthcare Provider Instructions. . . . . . . . . . . . . . . . . . . . . . . . . . 6 Testing Oxygen Concentration. . . . . . . . . . . . . . . . . . . . . . . . . . 19
IMPORTANT PARTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 Testing Inspiratory Trigger Sensitivity. . . . . . . . . . . . . . . . . . . . . 19

SET UP AND OPERATING INSTRUCTIONS . . . . . . . . . . . . . . . . . 7 FIGURES, DIAGRAMS AND PARTS LIST

POWER OPTIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 125 Portable Oxygen Concentrator Views. . . . . . . . . . . . . . . . . 20
Parts and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
BATTERY OPERATION AND CHARGING
Pneumatic Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Initial Battery Charge . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
ORDERING INFORMATION AND RETURN
Battery Charging. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Ordering Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Typical Battery Recharge Time. . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Return of Units. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Battery Charge Level . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Discharging Battery Bar Table (unplugged) . . . . . . . . . . . . . . . . 10 SPECIFICATIONS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
TRAVELING WITH THE IGO2 POC. . . . . . . . . . . . . . . . . . . . . . . . 10 ELECTROMAGNETIC COMPATIBILITY INFORMATION. . . . . . . 26
Electromagnetic Compatibility Compliance Levels. . . . . . . . . . . 27
MAINTENANCE. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Alarm System Function Check. . . . . . . . . . . . . . . . . . . . . . . . . . 11
Expected Service Life. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Information Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Entering Information Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Exiting Information Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
iGo2 POC Care and Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Exterior Cover & Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Carrying Case. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Power Supply, AC Power Cord, DC Power Cord. . . . . . . . . . 12
Cannula and Tubing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Cleaning & Disinfection When There is a Change of Patient.12
Return and Disposal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Disposal of Lithium-ion Batteries . . . . . . . . . . . . . . . . . . . . . . 13
TROUBLESHOOTING & ALARM SYSTEM
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Overview of Alarms. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
COMPONENT DESCRIPTION AND FUNCTION
Accumulator Manifold & Tank. . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Compressor. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Cooling Fan. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Dispense Valve. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Final Bacteria Filter. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Intake Filter (compressor silencer). . . . . . . . . . . . . . . . . . . . . . . 16
Molecular Sieve Beds. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Printed Circuit Board. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Purge Valve. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Switching Manifold . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

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 GE NE R A L I N F O R M ATI O N

SYMBOL DEFINITIONS
Danger - No smoking near patient or
device. Direct Current (DC
Power Button Alarm Silenced
 his symbol has a red circle and
T Power)
diagonal bar on the product label.
It is mandatory to read and understand
the operating instructions prior to use. Class II electrical
Increase Prescription
protection – double TUV Rheinland
 his symbol has a blue background
T Setting Button
insulated C US

on the product label.

Do not use near heat or open flames.
Decrease Prescription
 his symbol has a red circle and
T Type BF applied part Manufacturer
Setting Button
diagonal bar on the product label.
Do Not Disassemble
Battery Status Indicator European
 his symbol has a red circle and
T Catalog Number
Symbol Representative
diagonal bar on the product label.
Use no Oil, Grease or Lubricants

This symbol has a red circle and Normal Oxygen (Green) Serial Number 0044 European Rep CE Mark
diagonal bar on the product label.
RTCA / DO-160G Section 21 Category M
and Section 20 Category T - The
manufacturer of this POC has determined
this device conforms to all applicable FAA No MR (MR Unsafe) Unsafe for Magnetic Resonance
acceptance criteria for POC carriage and Low Oxygen (Yellow)
Environment
use on board aircraft.
 ext shown with this symbol is red on
T
the product label.
General Warning
 his symbol is used throughout this
T Federal (U.S.A.) law restricts this device to sale by or on
Service Required (Red)
manual to indicate hazardous the order of a physician
situations to avoid.
Important Information
 his symbol is used throughout this
T IP22 Ingress Protection - Protected against finger access to hazardous parts; protected against
manual to indicate important IP22 vertically falling water drops when enclosure is tilted up to 15°
information you should know.
Note and Information Symbol
 his symbol is used throughout this
T This device contains electrical and/or electronic equipment that must be recycled per EU
manual to indicate notes, useful tips, Directive 2012/19/EU- Waste Electrical and Electronic Equipment (WEEE)
recommendations and information.

Battery Pack Markings

Attention, Consult Instruction Guide UL Recognized for Canadian and Dispose of this product according to local
US market regulations.
For Canada & USA: Please call 1-800-822-
Refer to Operating Instructions Recycling Symbol Taiwan 8837 for information on how to recycle this
battery
Mark of conformity to applicable UN Transportation Test China RoHS
European Directives
Regulatory Compliance Mark of Recycling Symbol Regulatory Compliance Mark of Japan
Australia and New Zealand. Li-ion

Battery Charge Status Gauge

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IMPORTANT SAFEGUARDS
Read this entire guide before using your Drive DeVilbiss iGo2 portable oxygen concentrator. Important safeguards are indicated throughout this guide; pay
special attention to all safety information. Imminently and potentially hazardous information is highlighted by these terms:

DANGER
Indicates an imminently hazardous situation which could result in death or serious injury to the user or operator if not avoided.

WARNING
Indicates a potentially hazardous situation which could result in death or serious injury to the user or operator if not avoided.

CAUTION
Indicates a potentially hazardous situation which could result in property damage, injury, or device damage if not avoided.

IMPORTANT
Indicates important information you should know.

NOTES
Indicates notes, useful tips, recommendations, and information.

Read All instructions before Using.

IMPORTANT
The device is to be used only on the instruction of a licensed physician. It is intended for the administration of supplemental oxygen to oxygen
patients > 10 kg as indicated by the physician. It is a transit-operable and body-worn device, and is not intended to be used with other medical
devices. The device is not intended for life support, nor does it provide any patient monitoring capabilities.

WARNING
• Electric Shock Hazard – Do not use while bathing.
• Electric Shock Hazard – Do not immerse this device into water or any other liquid.
• Electric Shock Hazard – Do not attempt to open or remove the cover; there are no user-serviceable internal components. If service is required,
contact your equipment provider for instructions on obtaining service. Opening or attempting to service your device will void the warranty.

DANGER
• DANGER-NO SMOKING
• Oxygen causes rapid burning. Smoking during oxygen therapy is dangerous and is likely to result in facial burns or death. Do not allow smoking
within the same room where the oxygen concentrator or any oxygen carrying accessories are located. Do not smoke while your oxygen
concentrator is operating, or when you are near a person utilizing oxygen therapy.
• If you intend to smoke, you must always turn the oxygen concentrator off, remove the cannula and leave the room where either the cannula or
mask or the oxygen concentrator is located. If unable to leave the room, you must wait 10 minutes after you have turned off the oxygen
concentrator before smoking.
• There is a risk of fire associated with oxygen enrichment during oxygen therapy. Do not use the oxygen concentrator or accessories near sparks
or open flames.
• Open flames during oxygen therapy are dangerous and are likely to result in fire or death. Do not allow open flames or hot, sparking objects
within 2 m (6.5 feet) of the oxygen concentrator, cannula, or any oxygen carrying accessories.
• Oxygen makes it easier for a fire to start and spread. Do not leave the nasal cannula or mask on bed coverings or chair cushions if the oxygen
concentrator is turned on but not in use; the oxygen will make the materials flammable. Turn the oxygen concentrator off when not in use to
prevent oxygen enrichment.
• To prevent high concentrations of oxygen:
• Do not leave device running when not in use. Do not leave cannula unattended while unit is delivering oxygen. High concentrations of oxygen
can cause rapid burning.
• Keep the equipment in a well-ventilated area.

CAUTION
• Drive DeVilbiss recommends for optimal service life that the iGo2 Portable Oxygen Concentrator be operated for at least 30 minutes after it is
powered on. Shorter periods of operation, operating in extreme temperature/humidity conditions or in the presence of contaminates, and/or
handling and storage conditions outside those specified, may affect the long term reliable operation of the product.

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WARNING
• Position your unit near an electrical outlet at least 6 inches (16 cm) from walls, draperies, or any other objects that might prevent the proper flow
of air in and out of your device. The iGo2 concentrator should be located so as to avoid pollutants or fumes, and placed in a well-ventilated place
so that the air inlet and exhaust are not blocked. Do not cover unit with a blanket, towel, quilt, or other covering, as the unit may overheat.
• Do not lubricate fittings, connections, tubing, or other accessories of the oxygen concentrator to avoid the risk of fire and burns. No lubricants are
recommended for use on this device.
• Use only water-based lotions or salves that are oxygen-compatible before and during oxygen therapy. Never use petroleum or oil-based lotions or
salves to avoid the risk of fire and burns.
• The Drive DeVilbiss iGo2 portable oxygen concentrators are equipped with a fire mitigating outlet fitting that prevents propagation of fire into the
unit.
• See instructions for use regarding fire propagation prevention.
• Improper use of the power cord and plugs can cause a burn, fire, or other electric shock hazards. Do not use the unit if the power cord is
damaged.
• Locate oxygen tubing and power supply cords to prevent tripping hazards and reduce the possibility of entanglement or strangulation.
• Use only spare parts recommended by the manufacturer to ensure proper function and to avoid the risk of fire and burns.
• Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide.
• When device is used under extreme operating conditions, the temperature near the exhaust vents on the bottom of the unit may reach 57˚C
(134.6˚F). Keep bare skin away from this area.
• The following surface temperatures may exceed 41˚C (105.8˚F) under extreme conditions:
• External surface of POC............................. 52˚C (125.6˚F) • External power supply............................43˚C (109.4˚F)
• Exhaust gas at discharge port.................... 53˚C (127.4˚F) • Battery Pack ..........................................49˚C (120.2˚F)
Keep bare skin away from this area.

WARNING
• If you feel discomfort or are experiencing a medical emergency while undergoing oxygen therapy, seek medical assistance immediately to avoid
harm.
• Geriatric, pediatric or any other patient unable to communicate discomfort can require additional monitoring and/or a distributed alarm system to
convey the information about the discomfort and/or the medical urgency to the responsible caregiver to avoid harm.
• Use of this device at an altitude above 3000 meters (9843 feet) or above a temperature of 35˚C (95˚F) or greater than 93% relative humidity is
expected to adversely affect the flow rate and the percentage of oxygen and consequently the quality of the therapy. Refer to specifications for
details regarding parameters tested.
• The oxygen delivery setting has to be determined for each patient individually with the configuration of the equipment to be used, including
accessories. It is very important to follow the prescription determined by your physician.
• Your delivery settings of the oxygen concentrator should be periodically reassessed for the effectiveness of therapy.
• To ensure you receive the therapeutic amount of oxygen delivery according to your medical condition, the iGo2 oxygen concentrator must:
•  be used only after one or more settings have been individually determined or prescribed for you at your specific activity levels.
•  be used with the specific combination of parts and accessories that are in line with the specification of the concentrator manufacturer and that
were used while your settings were determined.
• The settings of this iGo2 portable oxygen concentrator do not correspond with continuous flow oxygen device settings.
• The setting of other models or brands of oxygen therapy equipment do not correspond with the settings of this iGo2 portable oxygen
concentrator.

WARNING
• The proper placement and positioning of the prongs of the nasal cannula in the nose is critical to the amount of oxygen delivered to the
respiratory system of the patient.
• Some respiratory efforts of the patient might not trigger the conserving equipment.
• Wind or strong draughts can adversely affect accurate delivery of oxygen therapy.
• This device is not intended for use with a tracheotomised patient.

WARNING
• To avoid electric shock, do not remove the concentrator cover. The cover should only be removed by a qualified Drive DeVilbiss technician. Do
not apply liquid directly to the cover or utilize any petroleum-based solvents or cleaning agents.
• Before attempting any cleaning procedures, turn the unit “Off” and disconnect from AC or DC power.
• Do not service or clean this device while in use with a Patient.
• Use no lubricants, oils or grease.
• Use of harsh chemicals (including alcohol) is not recommended. If bactericidal cleaning is required, a non-alcohol based product should be used
to avoid inadvertent damage.

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 GE NE R A L I N F O R M ATI O N

WARNING
• This device contains electrical and/or electronic equipment. Follow local governing ordinances and recycling plans regarding disposal of device
components.
MR Unsafe
• Do not bring the device or accessories into a Magnetic Resonance (MR) environment as it may cause unacceptable risk to the patient or damage
to the iGo2 or MR medical devices. The device and accessories have not been evaluated for safety in an MR environment.
• Do not use the device or accessories in an environment with electromagnetic equipment such as CT scanners, Diathermy, RFID and
electromagnetic security systems (metal detectors) as it may cause unacceptable risk to the patient or damage to the iGo2. Some
electromagnetic sources may not be apparent, if you notice any unexplained changes in the performance of this device, if it is making unusual or
harsh sounds, disconnect the power cord and discontinue use. Contact your home care provider.
• This device is suitable for use in home and healthcare environments except for near active HF SURGICAL EQUIPMENT and the RF shielded
room of an ME SYSTEM for magnetic resonance imaging, where the intensity of Electromagnetic DISTURBANCES is high.
• Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is
necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
• Use of accessories and cables other than those specified or provided by the manufacturer of this equipment could result in increased
electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.
• Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30
cm (12 inches) to any part of the iGo2, including cables specified by the manufacturer. Otherwise, degradation of the performance of this
equipment could result.

WARNING
THE FOLLOWING BATTERY SAFETY WARNINGS MUST BE OBSERVED AT ALL TIMES:
• Do not drop, hit, crush, or otherwise abuse the battery as this may result in the exposure of the cell contents, which are corrosive.
• Do not subject battery to mechanical shock.
• In the event of a battery leaking, do not allow the liquid to come in contact with the skin or eyes. If contact has been made, wash the affected
area with copious amounts of water and seek medical advice.
• Do not expose the battery to fire or extreme heat. Do not incinerate. Exposure of the battery to extreme heat may result in an explosion. Avoid
storage in direct sunlight.
• Do not expose the battery to water, rain or moisture of any type.
• Do not expose to water, fire or excessive heat.
• Do not crush, disassemble, puncture or short circuit the connector terminals.
• Do not open, disassemble, or attempt to repair the battery; there are no user-serviceable parts inside.
• Do not short-circuit battery.
• Do not store batteries haphazardly in a box or drawer where they may short circuit each other or be short-circuited by other metal objects.
• Keep batteries out of the reach of children.
• Keep batteries clean and dry.
• Use only the battery in the application for which it was intended.
• Periodically inspect connection cords, connector tips and the power supply for damage or signs of wear. Discontinue use if damaged.
• Charge the battery before initial use.
• Recommended maximum time between charges = 1 year
• Recommendation: Store the battery below 25°C (77°F), low humidity, no dust and no corrosive gas atmosphere. Store fully charged if possible.
• This device contains electrical and/or electronic equipment. Follow local governing ordinances and recycling plans regarding disposal of device
components.
• The battery must be recycled or disposed of properly.

Operating Principle
The Oxygen Concentrator uses molecular sieve to remove the nitrogen from ambient air and allow oxygen to remain in the air delivered to the patient. The
device is a pulse only oxygen concentrator which only delivers oxygen when a patient breath is detected.
Technical Description
Pulse Only Pressure Vacuum Swing Adsorption (PVSA), oxygen concentrator based on molecular sieve technology. Beds are evacuated and drawn down by a
compressor to a vacuum level, which is dependent on setting. Ambient air is then pumped into the concentrator through a series of filters that remove dust and
other particulate. A valve directs air into one of two sieve beds. Nitrogen is adsorbed in the bed as the pressure increases while oxygen flows through, thereby
producing a highly enriched oxygen product. Air is processed in the second bed out of phase in the cycle with the first bed. This allows processed oxygen to be
used in the cycle and to be delivered to the patient. Oxygen is provided to the patient only with pulse-dose basis.
Healthcare Provider Instructions
• The healthcare provider is responsible to determine oxygen delivery setting for each patient individually with the configuration of the equipment to be used,
including accessories.
• The healthcare provider is responsible to periodically reassess the delivery settings of the oxygen concentrator for the effectiveness of therapy.
• The healthcare provider is responsible to ensure the compatibility of the portable oxygen concentrator and all of the parts used to connect to the patient
before use.
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 I M PO RTA N T PA RTS

Important Parts of Your Concentrator

Drive DeVilbiss iGo2 Portable Oxygen Concentrator Oxygen
Outlet Port
Power Supply
(AC/DC Adapter) AC Power Cord
DC Power Cord
(Auto Adapter) Control
Panel

Battery/ Battery
Battery Bay Battery Connection
Terminals

USB Port
(not for
patient use)

Battery Charge Charge

Status Gauge Status
Exhaust Vents Power Input Serial Number/
Button
(both sides) Rating Label

Control Panel Overview

Decrease Prescription Increase Prescription
Setting Button Setting Button
Normal Oxygen
Symbol (green) – Prescription Setting
acceptable Standard Mode:
oxygen level (1 digit field). The device has 5 oxygen
Audible Alarm settings of 1 through 5.
Low Oxygen Silenced symbol (illu-
Symbol (yellow)– minates when audible
below an alarm has been
acceptable silenced by pressing
oxygen level the power button)
Service Required
Symbol (red) – Power Button
contact your SmartDose Mode:
provider when (2 digit field). The device has 4 oxygen settings of 1d
illuminated Initial Startup Screen through 4d where the d indicates SmartDose is enabled

Battery charge remaining

percentage (2-digit field) –
shows remaining charge as
percentage (99% max
shown)

Battery Status Indicator

NOTE– Press and hold either “+” or “-“ to
see battery charge remaining; display will
return to prescription setting in a few seconds.

Set Up and Operating Instructions

Refer to the instruction guide for set up and operating instructions.

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 P OW ER O PTI O N S

POWER OPTIONS 3. DC (car charger) Power.

Your iGo2 POC can be used on the 3 following power sources:
1. Battery Power – Your device must always have a battery installed to
operate. The iGo2 POC will use battery power if no other power source
is present. However, if AC or DC power is connected, the device will
run on that power source thus conserving battery charge level. If the
other power source is disconnected, the device will automatically switch
to battery power. The device will operate for a minimum of 3.5 hours at
a setting of 2 at 20 BPM (breaths per minute) using a new fully charged
battery.
a. START YOUR VEHICLE.
NOTE– DO NOT leave the iGo2 or Power Supply plugged into
the vehicle without the engine running or attempt to start the
vehicle while either is connected to the vehicle. This may drain the
vehicle’s battery.
b. Attach Power Supply to the device and to the vehicle accessory
power port using the DC power cord.
c. Secure the iGo2 POC and Power Supply in your vehicle and make
sure the air inlet and exhaust vents are not blocked.
NOTE– Battery will not charge if plugged into power source less than
13.8V but the device will function correctly.

2. AC Power (for use at home or where standard AC power is available) –

Attach the universal AC Power Supply to the concentrator and an AC
power outlet using the AC Power Cord.

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 BAT T E RY OP E R ATI O N A N D C H A RG I N G
Battery Battery Charging
To check the battery charge level percent, press and hold either the“+” or During charge, the battery status indicator blinks while the battery is
“-“ button, and the percent of battery remaining display will be shown. charging; it stays on solid when battery is not charging.
The display will revert back to prescription setting in a few seconds, but To charge iGo2 portable concentrator battery:
the battery status indicator is always shown.
1. Using AC Power - Attach the power supply to the concentrator and
an AC power source using the appropriate power cord.
2. Using DC Power - Your iGo2 includes a DC Cord that allows the
concentrator to operate from DC accessory power port outlets such
as those found in motor vehicles.
a. START YOUR VEHICLE.
NOTE– DO NOT leave the iGo2 or Power Supply plugged
into the vehicle without the engine running or attempt to start
the vehicle while either is connected to the vehicle. This may
drain the vehicle’s battery.
The iGo2 concentrator will operate for a minimum of 3.5 hours at a b. Attach Power Supply to the concentrator and to the vehicle
setting of 2 at 20 BPM (breaths per minute) using a new fully charged accessory power port using the DC power cord.
battery. c. Secure the iGo2 POC and Power Supply in your vehicle and
make sure the air inlet and exhaust vents are not blocked.
NOTE– The battery may have 75% of its initial capacity after 300
NOTE– Battery will not charge if plugged into power source less than
charge/discharge cycles; in this case, you can expect up to 2.5 hours of
runtime at a setting of 2 and 20 BPM. 13.8V but the device will function correctly.
NOTE– A separate battery charging station is also available for
Initial Battery Charge purchase.
Before using the device on battery power for the first time, the battery
needs to be fully charged. Optional spare batteries purchased should
Typical Battery Recharge Time
also be fully charged before first use. The typical time to recharge your battery from a fully discharged
condition is less than 5 hours dependent upon the setting.
1. To charge iGo2 portable concentrator battery, simply attach the
power supply to the device and an AC or DC power source using NOTE– Battery will charge in less than 3 hours from fully discharged
the appropriate power cord. state with device off and plugged into AC power; or less than 4 hours
when using DC power. While using the concentrator, charge time will be
2. The battery status indicator blinks to show charge level while the
less than 5 hours from fully discharged state using either AC or DC
battery is charging, and stays on once battery is fully charged
power.
(99%).
NOTE– Battery will not charge if plugged into power source less than
NOTE– If you purchased spare batteries for backup, insert into the
13.8V but the device will function correctly.
concentrator one at a time and charge as above.

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 BAT T E RY C H A RG I N G / TR AV EL

Battery Charge Level

Display (installed battery) Spare Battery (not installed)
To check the battery charge level percent, press and hold either the “+” or “-“ To check the charge level on a spare battery, simply press the Charge
button, and the percent of battery remaining display will be shown. The display Status Button on the individual battery.
will revert back to prescription setting in a few seconds, but the battery status
indicator is always shown.

Flashing = 10% remaining Flashing = 10% remaining

Audible Alert = 5% remaining NOTE– Each segment of the battery charge status gauge indicates 25%
Device Shutdown = within 2 minutes of reporting 5% charge
remaining. Plug in device or change battery to continue use.
of total charge capacity.

NOTE– Each segment of the battery charge status gauge indicates a percent
of the total charge capacity

Discharging Battery Bar Table (unplugged)

Battery Bar Display
Battery Charge Status Displayed Charge # of Bars Lit
90 - 100% 90 - 99 5 bars steady
70 - 89% 70 - 89 4 bars steady
50 - 69% 50 - 69 3 bars steady
30 - 49% 30 - 49 2 bars steady
11 - 29% 11 - 29 1 bar steady
6 - 10% 06 - 10 1 bar blinking at 1 Hz (slow flash)
1 - 5% 01 - 05 1 bar blinking at 3.3 Hz (fast flash)
*Device will shutdown within 2 minutes
of reporting 5% charge remaining

TRAVELING WITH THE IGO2 POC

Refer to the instruction guide for information and recommendations on traveling with the iGo2 POC.

LT-2334 10
 M A I N TENA N C E

MAINTENANCE
There is no routine or scheduled maintenance required for the iGo2 POC.

Alarm System Function Check

The alarm system function is checked automatically each time the unit is turned on. Therefore there is no monitoring system or method required to check the
function of the alarm system. At power on, the audible alarm sounds for 1 second and all LCD (liquid crystal display) segments light for 3 seconds to verify that
all LCD segments are operating.

Expected Service Life

• Oxygen Concentrator - 5 years
• Carrying Case - 5 years
• Compressor - 3 years
• Sieve Beds - 1 year
• Battery - 1 year
Expected service life of the unit, and in particular the sieve beds and compressor, may vary based on the operating environment, storage, handling, and the
frequency and intensity of use.
There is no portion of the gas pathways through the concentrator that could be contaminated with body fluids under normal or single fault.
The device patient connection may unintentionally become contaminated with expired gasses if a hose internal to the device, between the dispense valve and
patient outlet port, becomes disconnected. This would allow open flow from the patient to the device. A bacteria filter is used in the patient connection, and this
will prevent contamination of the system. The design of the concentrator allows removal of the patient connection for cleaning and/or replacement of the filter

INFORMATION MODE
Information mode allows you to view the Hour Meter and Serial Number.

Entering Information Mode

With the device plugged in and OFF:

- Press and hold all 3 buttons for 2 seconds until display shows Hour Meter.

Hr (Hour Meter)
Hr (Hour Meter) is displayed; it contains 5 digits shown across 3 segments. Display auto
scrolls through segments.

Press Power button for 1 second and release for Serial Number.

Sn (Serial Number)
Sn (Serial Number) is next item displayed; it contains 8 digits shown across 4
segments. Display auto scrolls through segments.

Exiting Information Mode

To Exit information Mode:

Press Power button for 2 seconds and release to exit Information Mode and turn off device.

NOTE– Information Mode times out after 2 minutes without user interaction.

11
LT-2334
 M A I N TENA N C E

IGO2 POC CARE AND CLEANING Carrying Case

The carrying case should be cleaned as needed. To clean, follow these
WARNING
steps:
To avoid electric shock, do not remove the concentrator cover.
1. Remove the device from the carrying case before cleaning.
The cover should only be removed by a qualified Drive DeVilbiss
technician. Do not apply liquid directly to the cover or utilize any 2. As needed, clean the case by using a damp cloth with a mild
petroleum-based solvents or cleaning agents. household cleaner and wipe dry.
Use of harsh chemicals (including alcohol) is not recommended.
If bactericidal cleaning is required, a non-alcohol based product
should be used to avoid inadvertent damage.
Use no lubricants, oils or grease.
Before attempting any cleaning procedures, turn the unit “Off” and
disconnect from AC or DC power.
Do not service or clean this device while in use with a Patient.

Exterior Cover & Battery

Power Supply, AC Power Cord, DC Power
Clean the concentrator exterior cover and battery as needed:
Cord
1. Ensure battery is installed while cleaning the cover.
1. Disconnect cords from the device and power source before cleaning.
2. Use a damp cloth or sponge with a mild household cleaner on the
exterior cover, and wipe it dry. If battery is removed, wipe battery bay 2. Clean the cords as needed by using a damp cloth with a mild
with a Dry Cloth only. household cleaner, and wipe dry.

CAUTION
Do not apply liquid directly to the cover.

Cannula and Tubing

Clean and replace the cannula and tubing according to the manufacturer’s
instructions.
3. Wipe battery with a Dry Cloth as needed.
Cleaning
Suggested Number of
cleaning cleaning Compatible cleaning
interval cycles * method
Outer Cabinet 7 days 260 Mild dish soap (2 tbsp)
and Battery and warm water (2 cups)
Power Supply 7 days 260 Mild dish soap (2 tbsp)
and Cords and warm water (2 cups)
Carrying Case 7 days 260 Mild dish soap (2 tbsp)
and warm water (2 cups)
* number of cleaning cycles determined by suggested cleaning interval and
expected service life

Cleaning & Disinfection When There Is A

Change Of Patient
The iGo2 POC should be cleaned and disinfected between patients as
follows:
1. Dispose of all accessories that are not suitable for reuse, particularly
the oxygen tubing and nasal cannula.

LT-2334 12
 M A I N TENA N C E

2. Clean the device, battery, and components as described in the Care

and Cleaning section.
3. Disinfect the surfaces of the device, battery, and components using
DisCide Ultra Towelettes by Palmero or equivalent and follow the
disinfectant manufacturer’s instructions. Avoid wiping the battery
terminals.
4. Remove the outlet port and filter under it, and discard. Replace with a
new filter and outlet port (part number 125D-610).
NOTE– The disinfection process can only be completed by the
manufacturer or by an appropriately trained individual.
Disinfection
Recommended Number of Compatible
disinfection disinfection disinfection
interval cycles method
Cabinet, power Between patients 60 DisCide Ultra
cords, carrying
case
Oxygen tubing, Do not clean, N/A N/A
nasal cannula, replace between
outlet port and patients
filter

RETURN AND DISPOSAL

This device may not be disposed of with household waste. After use of the
device, please return the device to the provider for disposal. This device
contains electrical and/ or electronic components that must be recycled per
EU Directive 2012/19/EU-Waste Electrical and Electronic Equipment
(WEEE). Non-infectious used accessories (e g nasal cannula) can be
disposed of as residential waste. The disposal of infectious accessories (e g
nasal cannula from an infected user) must be made via an approved waste
disposal company. Names and addresses can be obtained from the local
municipality.

Disposal of Lithium-ion Batteries

Lithium-ion batteries should be recycled. Some states have specific laws
regarding the disposal of lithium-ion batteries. You should contact your local
Government Household Hazardous Waste Agency for information on state
battery disposal regulations. For information on where you can recycle your
batteries at no cost, visit www.call2recycle.org or call 1-877-723-1297.
Recycle batteries according to national and local regulations. Contact your
local representative for assistance. The batteries must be disposed only in a
discharged state at the collection center. In case of not fully discharged
batteries, provide for a risk against short circuits. Short circuits can be
prevented by isolating the terminals with tape.

13
LT-2334
 T ROUBL E S HOOTI N G A N D A L A R M SYSTEM

TROUBLESHOOTING & ALARM SYSTEM

Troubleshooting
The following troubleshooting chart will help you analyze and correct minor malfunctions. If the suggested procedures do not help, switch to your reserve oxygen
system and call your Drive DeVilbiss homecare provider. Do not attempt any other maintenance.

WARNING
To avoid electric shock hazard, do not remove the covers. There are no user serviceable internal components. The covers should only be removed by
a qualified Drive DeVilbiss provider/Drive DeVilbiss homecare technician.

SYMPTOM POSSIBLE CAUSE REMEDY

Unit does not operate. Display is 1. Power button was not held. 1. Press Power button and hold for 2 seconds.
not illuminated and nothing 2. No battery installed 2. Battery must be installed for device to operate regardless of power
happens when Power button is source.
pressed and held.
3. Battery depleted or defective battery. 3. Install charged battery or contact provider for replacement
4. External power not attached and 4. Check cord connections to device, power supply, and power source.
battery is depleted.
5. No power at wall outlet. 5. Check your home circuit breaker and reset if necessary. Use a different
wall outlet if the situation occurs again.
6. Faulty Power Supply, AC Power Cord 6. Contact your Drive DeVilbiss provider
or DC Power Cord
7. Faulty DC accessory power port 7. Check automotive fuse.
outlet.
8. Unit malfunction 8. Contact your Drive DeVilbiss provider.
Unit is On; Audible Alert is 1. No breathing detected 1. Apply cannula and breathe on device.
sounding; No Visual Alarm 2. Cannula is not adjusted properly. 2. Check all cannula connections to make sure they are tight, and adjust the
cannula to fit comfortably in your nose. Ensure tubing is not kinked.
3. Tubing/cannula too long. 3. Replace with shorter tubing/cannula. Cannula and tubing length cannot
exceed 25’.
4. Low flow cannula being used. 4. Replace with standard cannula.
Cannot adjust/change the Oxygen 1. Unit malfunction. 1. Contact your Drive DeVilbiss provider.
Prescription setting.
Unit not triggering properly 1. Sensor needs recalibrated 1. Turn unit ON, but do not use it for 5 minutes to auto-calibrate the sensor.
Battery Fuel Gauge symbol is 1. Battery is nearing depletion. 1a. Charge Battery by connecting device to AC or DC power source.
flashing with or without Audible * Symbol flashes at <10% battery life. 1b. Install optional backup battery.
Alert * Audible Alert sounds at <5% battery Device will automatically shut down within 2 minutes of reporting 5% charge
life. remaining.
Yellow Low O2 symbol is flashing 1. Start Up period 1. Wait until startup period is done (about 10 minutes)
Yellow Low O2 symbol is On with or 1. The concentration of the unit is falling. 1. Contact your provider and switch to your reserve oxygen system.
without Audible Alert * Symbol flashes below 86%
* Audible Alert sounds below 85%
Red Service Required symbol 1. Unit Overheated 1. Ensure vent holes are not blocked. Allow unit to cool and try again.
flashes with Audible Alert 2. Unit malfunction 2. Contact your provider and switch to your reserve oxygen system.
Battery Status Lights Never 1. Using the DC auto adapter but there 1. Battery will not charge if plugged into power source less than 13.8V but
Indicate Fully Charged is not enough power to fully charge the device will function correctly.
battery.
Yellow Low O2 symbol is On and/or 1. Contaminated Sieve Beds 1. Run the unit for at least 15 minutes to recover sieve beds to full potential.
Red Service Required light is On 2. Replace sieve beds.
If any other problems occur with 1. Turn your unit Off and switch to your reserve oxygen system. Contact
your iGo2 POC. your Drive DeVilbiss provider immediately.

LT-2334 14
 T ROUBL E S HOOTI N G A N D A L A R M SYSTEM

Overview of Alarms
This device contains an alarm system which monitors the state of the device and alerts of abnormal operation, loss of essential performance or failures. Alarm
conditions are shown on the LCD display. The alarm system functions are tested at power up by lighting all visual alarm indicators and sounding the audible
alarm (beep). All alarms are Low Priority Technical Alarms.
To mute the Audible Alarm, press and release power button. The Alarm Silenced symbol will appear on the display until the alarm condition is corrected.

Alarm Display Visual Alarm Signal Audible Alarm Visual Alarm Signal
Condition Shows Meaning Signal Cleared by Action to take
Battery nears Battery is <10% Yes, when battery is < Turn off device or switch to Charge battery, change battery, or
depletion 5% alternate power source switch to alternate power source
Flashing
Low Oxygen Oxygen concentration is Yes, if oxygen drops Turn unit off unless the Call provider and switch to reserve
Concentration <86% below 85% device is still in startup oxygen.
period
Start-up period Device and systems are No Once oxygen reaches at Wait until startup is finished (up to
tested at power up least 86% 10 minutes)
Malfunction RED Service Required Yes Turn unit off Call provider and switch to reserve
symbol flashes indicating oxygen.
malfunction
No Breathing None More than 60 seconds Yes Turn unit off or breathe on Resume breathing. If no breathing
Detected between requested device. is detected, device will go into
dispense cycles. AutoBreath™ mode and dispense
oxygen at regular intervals until
breathing is detected again.

15
LT-2334
 COM P ONE NT DESC R I PTI O N A N D F U N C TI O N

COMPONENT DESCRIPTION AND Molecular Sieve Beds

FUNCTION Molecular sieve beds contain a synthetic alumino-silicate that attracts and
holds nitrogen in a magnetic bond. Two molecular sieve beds work in
Accumulator Manifold tandem: one bed removes nitrogen from the air passing through it while the
The accumulator manifold is mounted beneath the sieve beds and other bed releases the removed nitrogen back into the room air.
accumulator tank. It includes two check valves that are located between the Moisture or hydrocarbons contaminate molecular sieve material causing it to
outlet of each sieve bed and the accumulator tank. These check valves allow lose its nitrogen adsorbing properties, which in turn decreases the oxygen
oxygen to pass from the sieve beds to the accumulator tank, but prevent the concentration. To allow the iGo2 to exhaust these possible contaminants and
reverse flow of oxygen from the accumulator to the sieve beds. for optimal service life it is recommended that the unit is operated for a
minimum of 30 minutes after it is powered on.
Accumulator Tank
The accumulator tank holds the concentrated oxygen and releases it to the Shorter periods of operation, operating in extreme temperature/humidity
patient at a specified liter flow. conditions or in the presence of contaminates, and/or handling and storage
conditions outside those specified, may affect the long term reliable
Battery operation of the product.
The iGo2 uses a rechargeable lithium ion battery of 11.25 nominal volts, 6.4
Printed Circuit Board
amp-hours of total capacity and allows the iGo2 to operate free of connection
to an external power source. The iGo2 concentrator will operate for a The printed circuit (PC) board monitors and controls the operation of the
minimum of 3.5 hours at a setting of 2 at 20 BPM (breaths per minute) using iGo2. It cycles pressure and vacuum between the two sieve beds and
a new fully charged battery. However, a variety of factors such as age of initiates visible and audible alerts if abnormal operation is detected. The
battery and flow rate, can impact the duration of operating time. oxygen sensing device (OSD®) is located on, and controlled by, the PC
board.
After 300 charge/discharge cycles, the battery’s capacity may drop to about
75% of the original capacity; in this case, you can expect up to 2.5 hours of Purge Valve
runtime at a setting of 2 and 20 BPM. Before the switching manifold cycles pressure and vacuum to alternate sieve
Battery will charge in less than 3 hours from fully discharged state with beds, the PC board activates the purge valve briefly. During this time, the
device off and plugged into AC power; or less than 4 hours when using DC purge valve sends oxygen from the pressurizing bed to the evacuating bed
power. While using the concentrator, charge time will be less than 5 hours breaking any remaining nitrogen bonds and cleaning the bed in preparation
from fully discharged state using either AC or DC power. for its upcoming pressure cycle.

Compressor Switching Manifold

A dual-head compressor creates pressure and vacuum simultaneously and The switching manifold directs the pressure and vacuum created in the
is driven from a single brushless DC motor. The motor speed is regulated by compressor to the two sieve beds in alternating cycles. The cycle shift is
the printed circuit board. controlled by the PC board and occurs when a predetermined pressure is
reached in the accumulator tank.
Cooling Fan
The cooling fan provides a constant air flow to cool the compressor. A
defective cooling fan may cause the compressor’s internal thermo-protective
(thermal cut off) device to activate and shut the compressor off. Should this
condition occur the compressor will require several minutes for the thermo-
protective device to reset.

Dispense Valve
The dispense valve ensures that the selected flow rate is delivered (pulsed)
to the patient at each inhalation. When the PC board detects breathing it
activates or briefly opens the dispense valve to deliver the correct bolus of
oxygen for the selected flow rate at the beginning of inhalation.

Final Bacteria Filter

The final bacteria filter is located inside the oxygen outlet port. It prevents
contaminants from reaching the patient through the oxygen supply.

Intake Filter (compressor silencer)

The intake filter/silencer filters the air drawn into the compressor removing
particulate matter and also reduces the sound of the intake.

LT-2334 16
 S E RVI CI NG AND C O M PO N EN T R EPL AC EM EN T

POC SERVICING AND COMPONENT 5. Disconnect both the keypad (green) and LCD display (gold) ribbon
REPLACEMENT connectors from the pc board.

The 125 series POC requires no routine maintenance or servicing and there Disconnect Ribbon
is no specific testing required. However oxygen concentration and inspiratory Connector
trigger sensitivity can be checked if necessary. See page 19 for instructions Cover
on testing O2% and trigger sensitivity. Plate

There are a limited number of components that are serviceable or

replaceable in the field. This section includes step-by-step instructions for
removal and replacement of these components.
Tools and Equipment Needed:
• T-10 Torx driver 6. Loosen control panel label with a small instrument such as a narrow
• 5/16” Hollow core socket bladed flat head screwdriver and remove from cover plate.
• Oxygen analyzer
• Narrow bladed flat head screwdriver
Cover Loosen Label
To remove and replace cover:
1. Ensure that all power is removed from the unit including battery.
2. Lay the POC on its side with the battery cavity to the right side and the Cover Plate
USB port facing upward.
3. Using a T-10 torx screwdriver remove the 6 screws securing the cover.

Cover/Case 7. Remove backing and any back film from the new control panel label.
8. Slide the end of the ribbon connector through the hole in the cover
T-10 Torx plate.
Screwdriver 9. Align the label and seat it into place on the cover plate on top of the
LCD display.
10. Attach both the keypad and LCD display ribbon connectors to the pc
board.
11. Secure ribbons using plate restraint.
4. Carefully lift the cover off the unit and place it aside.
5. Replace the cover by placing it on top of the unit and secure with 6
screws (torque to 7 in-lbs).
Control Panel Label Cover Plate Restraint
To remove and replace control panel label:
1. Ensure that all power is removed from the unit including battery.
2. Remove cover from unit.
3. Disconnect the silicone oxygen tubing from the back of the oxygen
outlet port. 12. Position cover plate in case.
Disconnect Tubing from Oxygen Outlet Port 13. Re-attach the silicone oxygen tubing to the back of the oxygen port.
Re-attach Tubing

4. Lift cover plate up and out of case. Place it beside unit. 14. Replace cover.

17
LT-2334
 S E RVI CI NG AND C O M PO N EN T R EPL AC EM EN T

Oxygen Outlet Port and Final Bacteria Filter 5. Using a T-10 torx screwdriver, loosen the 2 screws at the top of the
To remove and replace oxygen outlet port and final bacteria filter: valve manifold of the sieve bed module.
1. Ensure that all power is removed from the unit including battery.
2. Using a 5/16” hollow core socket unscrew the oxygen outlet port by
turning counterclockwise and remove it from the unit.

5/16” Socket

Oxygen Outlet Port 6. Lift sieve bed module up several inches out of the retaining catches
and remove the valve manifold from the top of the sieve beds.

3. Install the new outlet port with final bacteria filter by turning clockwise
(torque to 9-10 in-lbs).

Oxygen Outlet Port

Final Bacteria Filter

7. Remove and discard the original sieve beds and all four rubber O-Rings
located at the top and bottom of each sieve bed.
NOTE– The O-Rings may remain on the valve manifold or in the
recesses of the accumulator tank.
Sieve Beds
To remove and replace sieve beds:
1. Ensure that all power is removed from the unit including battery.
2. Lay the unit on its side with the USB port facing upward.
3. Using a T-10 torx screwdriver, remove all 6 screws from the side case
and remove the case cover from unit.

Case Screws (6)

8. Uncap two new sieve beds and seat the bottom O-Rings (larger
O-Rings) on the bottom of each sieve bed, and the top O-Rings on the
aluminum manifold (smaller O-Rings). NOTE– 4 O-Rings are
included with each sieve bed package.
USB Port

4. Carefully lift the front display cover plate up and out of case. Place it
beside unit.

LT-2334 18
 S E RVI CI NG AND C O M PO N EN T R EPL AC EM EN T

9. Place sieve beds over accumulator tank assembly ports. Then rotate Testing Oxygen Concentration
beds until the bed is fully seated into position and so the serial number To test oxygen concentration:
is viewable. Be careful to prevent pinching the O-Rings during
1. Turn on the POC and adjust the oxygen delivery setting to 5.
assembly.
2. Allow the unit to run approximately 60 seconds until it goes into the
AutoBreath™ mode. This is indicated by a flashing oxygen symbol (low
or normal) on the display every 3 seconds accompanied by an audible
beep every 15 seconds.
NOTE– Pressing the power button will silence the audible alarm.
3. If the oxygen is low the yellow down arrow will flash and if the oxygen is
normal the green check mark will flash. It may take 1 or 2 minutes for
the oxygen concentration to reach specification.
4. When the normal oxygen symbol starts flashing the oxygen level has
Ports
reached specification and may be tested.
5. Attach a calibrated oxygen analyzer to the outlet port. Allow the oxygen
10. Gently lift the sieve beds and accumulator tank upwards to re-insert the concentration to stabilize on the analyzer before taking a final reading.
manifold onto the top of the sieve beds. Rotate the sieve beds slightly
while inserting to prevent pinching of the O-Rings. Testing Inspiratory Trigger Sensitivity
11. Re-install the 2 manifold screws (torque to 6-8 in-lbs). To test inspiratory trigger sensitivity:
1. Turn on the POC and adjust the oxygen delivery setting to 5.
2. Attach a standard oxygen cannula to the outlet port.
3. Pinch the tubing for 3 -4 seconds then release it and feel if a dose
(oxygen bolus) is delivered at the cannula nasal prongs. The green
normal oxygen symbol will also blink when a dose is delivered.
4. Testing may also be done at other flow settings if desired.
5. If the unit does not deliver a pulse of oxygen when the tubing is pinched
and released or if you suspect an issue with the units’ sensitivity, return
the unit for servicing.

12. Lift the front display cover plate back into the slots of the side case.

13. Ensure that no hoses or wiring harnesses are pinched and place the
side cover back onto the unit.
14. Re-install the 6 case screws (torque to 7 in-lbs).
15. Re-install the battery into the unit.

19
LT-2334
 F I GURE S , DI AG R A M S A N D PA RTS L I ST

125 PORTABLE OXYGEN CONCENTRATOR VIEWS

POC with Power Accessories

19-23

24

18

3
4

1 17

Final Bacteria Filter

(included with outlet port)

LT-2334 20
 F I GURE S , DI AG R A M S A N D PA RTS L I ST

12 11
10

9 8
7

15

14 13 16

21
LT-2334
 F I GURE S , DI AG R A M S A N D PA RTS L I ST

PARTS AND ACCESSORIES

125 POC
Part Description Part #
1 Oxygen Outlet Port w/Bacteria Filter 125D-610
2 Control Panel Label 125D-623
3 Cover Plate N/A
4 Case Screws (6) 125D-621
5 Cover/Case N/A
6 Printed Circuit Board N/A
7 Compressor N/A
8 Accumulator Tank N/A
9 Sieve Beds 125D-619
10 Cooling Fan N/A
11 Purge Valve N/A
12 Accumulator Manifold N/A
13 Switching Manifold N/A
14 Dispense Valve N/A
15 OSD (oxygen sensing device) N/A
16 Intake Filter (Compressor Silencer) N/A
ACCESSORIES
17 Battery 125D-613
18 Power Supply (120 Watt) DV68-620
19 AC Power Cord - USA DV51D-606
20 AC Power Cord – CE DV51D-607
21 AC Power Cord - UK DV51D-608
22 AC Power Cord – Australia DV51D-609
23 AC Power Cord - China DV51D-614
24 DC Power Cord DV6X-619
External Battery Charger – US 125CH-613
External Battery Charger – CE 125CH-614
External Battery Charger - UK 125CH-615
Carrying Case 125D-670

There are many types of oxygen tubing and cannulas. Certain accessories
may impair the device’s performance. Use only standard nasal cannula with
25’ or less of crush-proof oxygen tubing with this concentrator. Do not use
pediatric (low-flow) nasal cannula or mask. Your homecare provider should
also give you advice on the proper usage, maintenance, and cleaning.

LT-2334 22
 Pressure Sensor

O2 Sensor
Oxygen Outlet Port
(Cannula Connection)
Dispense Final Bacteria Filter

Accumulator Valve

Breath Sensor
PNEUMATIC DIAGRAM

Mechanical Mechanical
Check Valve Check Valve

Purge
Valve

23
Bed 1 Molecular Bed 2
Sieve
Beds

2 2 2 2
Switching Switching
Valve 1 Valve 2 Mechanical
1 3 1 3 1 3 1 3
Check Valve
F I GURE S , DI AG R A M S A N D PA RTS L I ST

Vacuum Dump
P MTR V

Vacuum Sensor

Intake
Filter Orifice Exhaust

LT-2334
 ORDE RI NG I NFO R M ATI O N A N D R ETU R N

ORDERING INFORMATION
When ordering components, instruction guides, or service manuals the following must be provided:
• Unit Catalog Number
• Unit Serial Number
• Part Number
• Quantity Required
Drive DeVilbiss iGo2 Portable Oxygen Concentrator Instruction Guide:
• A-125 125D, 125K & 125A English, Spanish, French
• SE-125-1 125D, 125K & 125A English, Spanish, French
• SE-125-2 125D, 125K & 125A German, Italian, Netherlands, Portuguese, Greek, Polish
• SE-125-3 125D, 125K & 125A Arabic, Hindi, Russian, Turkish
• SE-125-4 125D, 125K & 125A Danish, Finnish, Norwegian, Swedish
• SE-125-5 125D, 125K & 125A Japanese, Chinese (Simplified), Chinese (Traditional)
Drive DeVilbiss iGo Portable Oxygen Concentrator Service Manual:
• LT-2334 125D, 125K & 125A English
Orders may be placed by calling:
• Customer Service 800-338-1988
• International Department 814-443-4881
• Europe +49 (0) 621-178-98-0
Return of Units
Before returning units to the factory, call the Drive DeVilbiss Healthcare Customer Service Department (800-338-1988) or (814-443-4881) to obtain a return
authorization number. Include in the package a note indicating the return authorization number along with your company name, address, phone number, and
account number. The return authorization number should also be written on the outside of the package.
To expedite your order for non-warranty parts, the following information should be given to the representative:
• Catalog number
• Serial number
• Hour meter reading for each concentrator
• Account number
• Company name and address
• Description of problem

LT-2334 24
 S P EC I F I C ATI O N S

Dimensions (H x W x L).......................................................................................................................................................................8.4”H x 3.5”W x 8.6”L (21.3 cm x 8.9 cm x 21.8 cm)

Weight....................................................................................................................................................................................................................................4.95 ± 0.1 lb. (2.25 ± 0.05 kg)
Oxygen Output......................................................................................................................................................................................................... 90% + 4/-3 over entire operating range
Oxygen Prescription Settings........................................................................................................................................................................................................................................ 1 to 5
Operating Temperature Range...................................................................................................................................................................................... +5 °C to +35 °C (+41 °F to +95 °F)
Operating Humidity Range....................................................................................................................................................................................................15 % to 93 %, non-condensing
Operating Atmospheric Pressure Range............................................................................................................................................................... 700 hPa to 1060 hPa (up to 10,000 feet)
Transport & Storage Temperature Range................................. - 20 °C (-4 °F) without relative humidity control to +60 °C (+140 °F) at a relative humidity up to 93%, non-condensing
Transport & Storage Humidity Range...................................................................................................................................................................................... 15% to 93% non-condensing
Transportation and Storage Atmospheric Pressure (at nominal temperature and humidity) ............................................................................................................... 640 hPA - 1060 hPA
Inspiratory Trigger Sensitivity.............................................................................................................................................................................................................................. 0.05 cmH20
Maximum Limited Pressure...........................................................................................................................................................................................................................................24 psi
Maximum Breathing Rate ........................................................................................................................................................................................................................................ 40 BPM
Sound Level.....................................................................................................................................................................................................................< 37 dBA at setting 2 and 20 BPM
(when measured at 1 m from front of device)
Measured Sound Pressure Level (ISO 80601-2-69:2014).......................................................................................................................................................................................< 40 dBA
Measured Sound Power Level (ISO 80601-2-69:2014)...........................................................................................................................................................................................< 48 dBA
Measured Sound Pressure Level Range of Alarm (IEC 60601-1-8:2012)...............................................................................................................................................................> 59 dBA
Power Quality Requirements
AC Mains Input................................................................................................................................................................................................................... 100-240 VAC, 50/60 Hz, 140 VA
DC Input....................................................................................................................................................................................................................................................... 13.8 to 17 VDC
The battery will charge as long as the DC input voltage is higher than the battery voltage. The device will charge the battery to full capacity if the DC input is at or above 13.8V DC.
OSD Set Points.....................................................................................................................................................................................................≥ 86% - Normal Oxygen Symbol (Green)
< 86% - Low Oxygen Symbol (Yellow)
< 85% - Service Required Symbol (red) and Audible Alert
Device Classification ....................................................................................................................................................................................................Class 2, Type BF Applied Part, IP22
The Drive DeVilbiss iGo2 Portable Oxygen Concentrator meets RTCA DO-160G Section 21 Category M and Section 20 Category T Airline Use.
Patented Breath Sensing with SmartDose Technology – US 8061353
Patented PulseDose Technology – US 4519387 and US 4457303

CAUTION
When moving the iGo2 POC from an extreme environment, allow time for the device to acclimate to the recommended operating environment. Operating
your concentrator outside the recommended operating environment may impact performance, cause damage, and will void the warranty.

Specifications subject to change without notice.

Audible Alerts:
• Low Battery
• Low Oxygen Output
• No Breath Detected
• Unit Malfunction
Table 1 – Standard and SmartDose® Mode PulseDose® Output
Standard and SmartDose Mode Oxygen Bolus Dispense Table
Fixed Minute Volume per Bolus Volume Bolus Volume Bolus Volume
Setting Setting (ml) @ 10 BPM (ml) @ 20 BPM (ml) @ 25 BPM (ml)
1 260 26.0 13.0 10.4
2 440 44.0 22.0 17.6
3 725 72.5 36.3 29.0
4 880 88.0 44.0 35.2
5 1014 101.4 50.7 40.6

Per ISO 80601-2-67

+/-15% at Standard Temperature and Pressure (tested @~933 hPa, 25 ˚C +/- 5 ˚C)
+/-25% over entire operating range
The above chart shows oxygen output delivered at each of the settings during normal use. When SmartDose technology senses the need for more oxygen, your
oxygen setting will temporarily be increased by up to 1 setting to help keep you active and saturated.

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If the device performance is lost or degraded due to electromagnetic disturbances, a visual and audible alarm indicates that the device is not meeting
specification or a failure has been detected.

WARNING
MR Unsafe
Do not bring the device or accessories into a Magnetic Resonance (MR) environment as it may cause unacceptable risk to the patient or damage to
the iGo2 or MR medical devices. The device and accessories have not been evaluated for safety in an MR environment.
Do not use the device or accessories in an environment with electromagnetic equipment such as CT scanners, Diathermy, RFID and electromagnetic
security systems (metal detectors) as it may cause unacceptable risk to the patient or damage to the iGo2. Some electromagnetic sources may not
be apparent, if you notice any unexplained changes in the performance of this device, if it is making unusual or harsh sounds, disconnect the power
cord and discontinue use. Contact your home care provider.
This device is suitable for use in home and healthcare environments except for near active HF SURGICAL EQUIPMENT and the RF shielded room of
an ME SYSTEM for magnetic resonance imaging, where the intensity of Electromagnetic DISTURBANCES is high.

WARNING
Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is
necessary, this equipment and the other equipment should be observed to verify that they are operating normally.

Cables and maximum lengths of cables

• DC power cord (cigarette lighter adapter) #DV6X-619 maximum length = 2.2 meter (7.2 ft)

WARNING
Use of accessories and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic
emissions or decreased electromagnetic immunity of this equipment and result in improper operation.

WARNING
Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm
(12 inches) to any part of the iGo2, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment
could result.

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Electromagnetic Compatibility Compliance Levels

TEST DESCRIPTION SPECIFICATION NOTES RESULTS
IEC 60601-1-2:2014 (4th Edition) / CISPR 11 / FCC Part 15 / RTCA/DO-160G / EN 55011:2010
Conducted Emissions EN 55011:2009+A1:2010 Class B Complies
150kHz – 30MHz
Conducted Emissions FCC Part 15, Subpart B Class B Complies
150kHz – 30MHz
Radiated Emissions CISPR 11 / Class B Complies
EN 55011:2009+A1:2010 30MHz – 1GHz
Radiated Emissions FCC Part 15, Subpart B Class B Complies
150kHz – 30MHz
Harmonic Current Emissions EN 61000-3-2:2014 AC Input ≤16Amps Complies
Voltage Fluctuations & Flicker EN 61000-3-3:2013 AC Input ≤16Amps Complies
Electrostatic Discharge Immunity EN 61000-4-2:2008 ±2kV, ±4kV, ±8kV, ±15kV (Air) Complies
8kV (Contact)
Radiated Electromagnetic Field EN 61000-4-3:2010 80MHz to 2.7GHz @ 10V/m; Complies
Immunity 80% AM at 1kHz
Proximity Fields from RF Wireless EN 61000-4-3:2010 385 MHz – 5785 MHz Complies
Pulse Modulation @ 18Hz and 217 Hz
Test Levels
9V/m and 28V/m
Fast Transient/Burst Immunity EN 61000-4-4:2012 ±2kV for Power Lines & ±1kV for I/O Complies
Lines
Surge Immunity EN 61000-4-5:2014 ±0.5kV, ±1kV & ±2kV (L-PE and N-PE) Complies
and ±0.5kV & ±1kV (L-N) @ 0°, 90°
and 270°
Conducted RF Immunity EN 61000-4-6:2013 150kHz to 80MHz @ 3Vrms Complies
6V in ISM and Amateur Radio bands
between 150kHz-80MHz
80% AM at 1kHz
Magnetic Field Immunity EN 61000-4-8:2009 30A/m @ 50Hz & 60Hz Complies
Voltage Dips, Short Interruptions & EN 61000-4-11:2010 >95%/0.5 cycle Complies
Variations 60%/5 cycles
30%/25 cycles
>95%/5 seconds
Radiated Susceptibility RTCA/DO-160G Category M Complies

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 Drive DeVilbiss Healthcare
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USA
800-338-1988 • 814-443-4881

Drive DeVilbiss Healthcare Ltd. Australian Sponsor:

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D e Vi l b i ss H eal t hcare LLC • 100 De Vilb iss Dr ive • S o me r set, PA 15 5 0 1 • USA

800-338-1988 • 814-44 3 - 4 8 8 1 • www.DeVilbissHea lthcar e .co m

DeVilbiss® iGo®2, PulseDose® and OSD® are registered trademarks of DeVilbiss Healthcare. AutoBreath™ is a trademark of Drive
DeVilbiss. SmartDose® is a registered trademark of Inovo.

© 2019 DeVilbiss Healthcare LLC. 08.19 All Rights Reserved. LT-2334 Rev. A