OxyGo OXYHOME 1400-5100 User manual

OXYGEN CONCENTRATOR
User Manual
Model: 1400-5100
RxOnly
Caution:Federal law restricts this device to sale by or on the order of aphysician. Read this instruction
manual carefully before use.

2
Contents
Glossary - Explanation of Packaging and Labelling Symbols.............................................................................3
Introduction...............................................................................................................................................................4
About OxyHome ....................................................................................................................................................4
General Information ..............................................................................................................................................4
How to Use this Manual........................................................................................................................................4
Intended Use..........................................................................................................................................................4
Contraindications and Precautions ....................................................................................................................4
Warnings Overview ..................................................................................................................................................5
Cautions Overview ...................................................................................................................................................6
Concentrator Features .............................................................................................................................................7
Front and Back of Concentrator..........................................................................................................................7
Side Panel ..............................................................................................................................................................7
Control Panel.........................................................................................................................................................8
User Controls.....................................................................................................................................................8
User Interfaces...................................................................................................................................................8
Indicator Lights..................................................................................................................................................8
Flow Meter..........................................................................................................................................................9
Oxygen Outlet Port............................................................................................................................................9
Accessories ...........................................................................................................................................................9
Operating Instructions .......................................................................................................................................... 10
General Instructions .......................................................................................................................................... 10
Cleaning, Care, and Maintenance ........................................................................................................................ 11
Routine Maintenance and Repairs ................................................................................................................... 11
Case Cleaning .................................................................................................................................................... 11
Cannula Replacement ....................................................................................................................................... 11
Filter Replacement ............................................................................................................................................. 11
Disposal of Equipment and Accessories ........................................................................................................ 11
Troubleshooting .................................................................................................................................................... 12
Product Specifications.......................................................................................................................................... 12
Environmental .................................................................................................................................................... 13
EMC Information .................................................................................................................................................... 13
TERMS AND CONDITIONS.................................................................................................................................... 17
Trademarks and Disclaimer .............................................................................................................................. 18
Trademark ....................................................................................................................................................... 18
Disclaimer ....................................................................................................................................................... 18
This Document................................................................................................................................................ 18
For Help ........................................................................................................................................................... 18

3
Glossary - Explanation of Packaging and Labelling Symbols
|
On (Power)
◯
Off (Power)
Refer to instruction
manual/booklet
Class II Device symbol
WARNING -
Statements that
describe serious adverse
reactions and potential safety
hazards.
CAUTION - Statements that call
attention to special care to be
exercised by the
practitioner/patient.
Serial Number
Operating atmospheric pres sure
Batch code
Humidity limitation
Type BF according to electrical
safety requirements
Storage temperature
No Open
Flames
No open flame when device is in
use or do not incinerate
U.S. federal law restricts this
device to sale by or on the order
of a physician
No Smoking
No smoking
Keep dry
Do not disassemble
(Contact your provider)
This side up
DO NOT use oil or grease
Stacking limit by number
Handle with care
Date of manufacture
Do not use if packaging is
damaged
Manufacturer
Separate collection for electrical
and electronic equipment

4
Introduction
The OxyHome 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. Please refer to this manual for detailed instructions on warnings, cautions,
specifications, and additional information.
About OxyHome
The OxyHome Oxygen Concentrator uses a pressure swing adsorption process and a molecular sieve to
separate and concentrate oxygen from the air. The device can provide a continuous flow of oxygen up to 5 LPM.
The concentration of supplied oxygen is from 93% + or –3%. The weight of the OxyHome Oxygen Concentrator is
41.8lbs (19kg).
General Information
This equipment is classified as:
•Class II
•Type BF
IMPORTANT: Users should read this entire manual before operating the OxyHome Oxygen Concentrator. Failure
to do so could result in personal injury and/or death. If you have questions about the information in this user
manual or about the safe operation of this system, contact your oxygen provider.
How to Use this Manual
This user manual contains warnings, cautions, and notes to help call attention to the most important safety and
operational aspects of the device. To help identify these items when they occur in the text, they are shown using
the following typographical conventions:
WARNING: Statements that describe serious adverse reactions and potential safety hazards.
CAUTION: Statements that call attention to information regarding any special care to be exercised by the
practitioner and/ or patient for the safe and effective use of the device.
IMPORTANT:Statements calling attention to additional significant information about the device or a procedure.
The Medical Devices Directive 93/42/EEC states that the product provider must ensure that all users of the device
are provided with the User Manual. The User Manual for this device has been written to account for training and
knowledge of the patient population to operate the device appropriately.
Intended Use
The OxyHome Oxygen Concentrator is for use by prescription only and intended to deliver concentrated oxygen
to adult patients with chronic pulmonary diseases, or any patient requiring supplemental oxygen. The OxyHome
Oxygen Concentrator may be used in a home environment or institutional environment. OxyHome is not intended
to be life-supporting or life-sustaining.
Contraindications and Precautions
The OxyHome Oxygen Concentrator is not intended to be used:
•In life-supporting or life-sustaining situations
•In an operating or surgical environment
•With a non-adult population
•In conjunction with the flammable anesthetic or flammable materials

5
Warnings Overview
1. Do not use the product without first reading the user manual.
2. Do not operate this device if unsure of its operation or function. Contact your home oxygen provider for
assistance or further information.
3. There is a risk of fire associated with oxygen equipment and therapy. Do not use near sparks or open
flames.
4. Geriatrics or any other patient unable to communicate discomfort can require additional monitoring to avoid
harm.
5. Smoking (including e-cigarettes) during oxygen therapy isdangerous and is likely to result infacial burns,
serious injury or death of the patient and others from fire. Do not allow smoking or open flames within
the same room astheoxygen concentrator orany oxygen carrying accessories.If you smoke, you
must always turn the oxygen concentrator off, remove the cannula and leave the room where either the
cannula or the concentrator islocated.
6. Use only water-based lotions that are oxygen compatible, before and during oxygen therapy. Never use
petroleum or oil-based lotions or salves when operating the device to avoid the risk of fire and burns.
7. Open flames during oxygen therapy are dangerous and are likely to result in fire or death. Do notallow
open flames within 3 meters (10 feet) of the oxygen concentrator or any oxygen carrying accessory.
8. Oxygen makes iteasier for a fire to start and spread. Do not leave the nasal cannula on bed coverings,
chair cushions or otherwise unattended with the concentrator on, but not in use; the oxygen will make the
materials flammable. Turn the concentrator off when not in use to prevent oxygen enrichment.
9. Explosion hazard. Do not use in the presence of flammable anesthetics, cleaning agents, or other
chemical vapors.
10. Do not use this device in the presence of pollutants or fumes.
11. Do not submerge this device in liquid. Do not expose to water or precipitation. Do not expose to dusty
conditions.
12. Do not use a device or any accessory that shows any sign of damage.
13. Do not use lubricants on this device or any of its accessories.
14. Use of this device at an altitude above 10,000 feet (3,000 m),or outside the temperature range of 41°F (5°
C) to 104°F (40°C), or outside the humidity range of 5% to95% may adversely affect the flowrate and
percentage of oxygen and consequently the quality of therapy. When not in use, the device should be
stored in a clean, dryenvironment between -13°F and 158°F (-25°C and 70°C). Use and/or storage outside
of the valid conditions may damage the product.
15. If feeling ill or are experiencing discomfort while using this device, contact your clinician or seek medical
assistance immediately to avoid harm.
16. Your home oxygen provider mustverify the compatibility of the device and all accessories used prior to
use. To ensure you are receiving the therapeutic amount ofoxygen for your medical condition, the device
and accessories mustonly be used after one of moresettings havebeen determined or prescribed for you
atyour specific activity levels by a healthcare professional.
17. The electrical cord and tubing could present a tripping or strangulation hazard. Keep away from children
and pets.
18. Do not disassemble or modify this device or any of its accessories. Do not attempt any maintenance other
than tasksdescribed in the Troubleshooting section.Disassembly can create an electric shock hazard and
will void the warranty. Contact your distributor for servicing by authorized personnel.
19. Use only spare parts recommended by the manufacturer to ensure proper function and to avoid the risk of
fire and burns.
20. Do not repair or perform service work while the device is in use by the patient.

6
Cautions Overview
1. Keep away from heat sources (fireplaces, radiant heaters, etc.) that could cause the operating temperature
at or near the device to exceed 104°F (40°C).
2. The display may be difficult to read under bright lighting conditions (sunlight, interior lights, etc.), move
away from direct light for viewing the display.
3. Keep away from lint or other loose material that could block the air intake vents.
4. Some countries restrict this device to be sold by or on an order of a prescribing clinician. Please ensure
you comply with relevant local laws.
5. Non-prescribed oxygen therapy can be hazardous under certain circumstances. Use this device only when
prescribed by a duly licensed clinician.
6. Always operate the device at the flow rate prescribed by a clinician. Do not alter the flow rate unless
prescribed by a clinician. Periodic reassessment of the flow settings should be done by a clinician.
7. It isrecommended for an alternate source of oxygen to be made available in the event of power outage or
mechanical failure. Consult your home oxygen provider or clinician for an appropriate backup system.
8. It isthe responsibility of the patient to make alternative or backup arrangements for oxygen when traveling.
9. This device may not reach specified oxygen concentration purity until ithas been in use for up to 2 minutes
at set flowrate.
10. This device is designed for use by one patient at a time.
11. The device can be re-used by a new patient. The device should be cleaned as indicated in this user
manual and, according to local laws and prescriptions prior to delivering to a new patient.
12. If you are unable to hear or see alarms or cannot communicate discomfort, consult a clinician before using
this device.
13. If oxygen concentration drops below the specified level, an alarm will indicate this condition. Ifalarm
persists, stop using this device, switch to an alternate source of oxygen, and contact your home oxygen
provider.
14. Only use approved accessories with this device. Using unapproved accessories may impair the
performance of this device.
15. Always follow the cannula manufacturer’s instructions for proper use.
16. Replace the cannula on a regular basis. Check with your home oxygen provider or clinician to determine
how often the cannula should be replaced.
17. Do not use cleaning agents other than those specified in this manual. Allow the cleaning solution to dry
from the cleaned surface before use.
18. Always turn off this device when not in use.
19. Do not use extension cords with power cord provided.
20. Always disconnect power and turn offthis device before cleaning, see “Cleaning, Care, and Maintenance.”
21. Do not obstruct air intake orexhaust vents when operating this device. Blockage can cause buildup of
internal heat and shut down or damage this device.
22. Do not place objects on top of this device.
23. Keep away from children and pets to prevent damage to the device and accessories and/ or inadvertent
setting changes.
24. Keep the device away from petsand pests.
25. Do not use in dusty or wet conditions.
26. Always use in a well-ventilated location.
27. If this device indicates an abnormal condition, see the Troubleshooting section.
28. Use caution when touching this device in high ambient temperatures.
29. The device can be isolated from power by disconnecting the power supply from the input connector.

7
Concentrator Features
Front and Back of Concentrator
Side Panel
Cabinet
Display
Oxygen Outlet Port
Flow Setting Knob
Humidifier Bottle
Flow Meter
Pause Button
Alarm On/Off
Timer
Switch On/Off
Top Handle
Built-in Filter Box
Universal Wheels
Oxygen Outlet Port
Circuit Breaker
Side Handle

8
Control Panel
User Controls
User Interfaces
Indicator Lights
There are 4 indicator lights on the device, please see below for descriptions.
1. Low outlet pressure indicator (Low Pressure): Outlet pressure is less than 2.2 psi, the indicator light
will flash yellow every two seconds and an alarm will sound.
2. Low oxygen purity indicator (Low Conc.): If the oxygen concentration drops below 82% (V/V) the
indicator light will flash yellow, and the alarm will sound.
3. Power loss indicator (Power Outage): When there is a power outage, the indicator light will flash yellow
every 2 seconds and the alarm will sound.
4. Power status indicator: When the concentrator ispowered on, the indicator light will remain solid green
if the concentrator is working normally.
Item
Description
Function
1
On / Off Switch
Press the switch to turn the device “On” or “Off”
2
Timer
After the device starts to deliver the oxygen, you can
set the treatment time by pressing and holding the
Timer button for 10 seconds. You can set the timer
from 10 minutes to 300 minutes in 10-minute
increments. After the timer setting expires, oxygen
delivery will be shutdown automatically.
3
Alarm On / Off
Press and hold this button for 10s to mute alarm sounds.
4
Pause Button
Press the button to pause oxygen delivery.
Item
Description
Function
5
Display
The LCD panel displays total running time, timer, and
alarm indicators. Alarm indicators will appear when
there is an error.
6
Indicator Lights
There are four indicator lights on the device, see table
below for descriptions.
7
Audible Signals
An audible signal (beep) indicates either a change in
operating status or a condition that may need
response (alert).
1
2
3
4
5
6
Low Pressure

9
Item
No. Alarm type Priority
Alarm Signals /Indicator light
Auditory
Yes/No
Alarm
condition
delay/ s
Alarm
signal
generation
delay/sColor
Flashing
frequency
Vacancy
ratio
1
Power supply failure
alarm Med Yellow
Flashing
every two
seconds50% Yes 5s 5s
2 Start-up fail alarm Med Yellow
Flashing
every two
seconds50% Yes 5s 5s
3
Low oxygen concentration
ALARM (non-startup) Med Yellow
Flashing
every two
seconds
50% Yes 5 s 5s
4 Pressure failure alarm Med Yellow
Flashing
every two
seconds
50% Yes 5 s 5s
Flow Meter
WARNING: Always operate the device at the flow rate prescribed byyour physician ortherapist. Do
not change theL/min setting on theflowmeter unless a change has been prescribed.
Rotate the knob on top of the flow meter to set the flow as prescribed by your physician or doctor. The position of
the black ball inside of the flow meter indicates the flow rate.
Oxygen Outlet Port
Connection port for cannula or humidifier bottle.
Accessories
CAUTION: Only use approved accessories with this device. The accessories listed below are
recommended for use with this device. The use of any other accessories which are not specified for
use with this device may reduce performance and void the manufacturer’s warranty. Contact your
distributor for updated information and accessories or if additional, optional, or replacement
accessories are needed.
Description
Part Number
User Manual
1170-5400
Cabinet Filter
1170-5401
Compressor Inlet Filter
1170-5402
HEPA Filter
1170-5403
Locking Wheel
1170-5404
Flow Control Knob
1170-5405

10
Necessary but not provided with this equipment – Nasal Cannula
There are many types of nasal cannulas that can be used with this device. Any FDA approved nasal cannula tube
can be used with continuous flow delivery and may be sized according to your prescription as recommended by
your homecare provider who should also give you advice on the proper usage, maintenance, and cleaning.
The use of FDA approved nasal cannulas are recommended (Product code: CAT, regulated by CFR 868.5340)
The nasal cannula is for single patient use.
CAUTION: Replace the cannula on a regular basis. Check with your home oxygen provider or
clinician to determine how often the cannula should be replaced. A nasal cannula must be used with
OxyHome to provide oxygen from the concentrator.
A humidifier is not included with the device. If you need humidification, please consult with your provider. If you
are using a humidifier, connect tubing from the concentrator’s oxygen outlet to the humidifier. Then connect the
supply tube/cannula to the humidifier.
For detailed usage, cleaning and disinfection of the oxygen supply tube and humidifier bottle, please refer
to their instruction or use provided by your supplier.
Operating Instructions
General Instructions
WARNING: Do not use the device or any accessory that shows any sign of damage.
1. Place the concentrator in a well-ventilated location.
The concentrator requires unobstructed ventilation. Ventilation ports are located at the bottom and back
of the concentrator. Place device a minimum of 6 to 12 inches away from walls, furniture, and curtains
which may impede air flow to the device.
2. Ensure both particle filters are in place.
CAUTION: Do not operate the device without the inlet filter and gross particle filter in place.
The concentrator may be damaged if used without these filters.
3. Connect the Power Supply
Connect the AC power plug to an electrical outlet.
CAUTION: Avoid the use of electrical extension cords with the concentrator. If an extension
cord must be used, please consult your Equipment Provider.
4. Connect the nasal cannula tubing to the oxygen outlet port.
5. Power on the concentrator by pushing the On/Off switch to On (|).
The power indicator light will turn solid green.
6. Set the concentrator to the flow prescribed by your physician.
Rotate the knob on the top of the flow meter to set the flow as prescribed by your physician or doctor.
7. Position the nasal cannula on your face and inhale the oxygen through your nose.
Place the nasal cannula over your ears and position the two prongs of the nasal cannula into your nostrils
to start oxygen therapy.
8. When not in use, turn off the concentrator by pushing the On/Off button to Off (◯).

11
Cleaning, Care, and Maintenance
Routine Maintenance and Repairs
The service life of the internal filters and sieve modules will depend on operating conditions. Do not attempt to
repair the device. Contact your home oxygen provider or distributor for assistance.
WARNING: Do not use oil, grease, or petroleum-based products on or near the Oxygen Concentrator or its
accessories.
CAUTION: Always disconnect power and turn off this device before cleaning. Do not disassemble or modify
this device or any of its accessories due todanger of electrical shock.
Case Cleaning
You may clean the outside case using a cloth dampened with a mild liquid detergent (Such as Dawn™) and
water.
Clean the exterior with a soft cloth slightly dampened with soapy water or with anti-bacterial wipes (Isopropyl
alcohol 70% solution). For disinfecting, use a wipe or equivalent and follow the manufacturer’s instructions.
Cannula Replacement
Your nasal cannula should be replaced on a regular basis. Consult with your physician and/or equipment
provider and/or cannula manufacturer’s instructions for replacement information.
CAUTION: Refer to the original manufacturer’s instruction for cleaning the nasal cannula.
Filter Replacement
The gross particulate filter located on top of the filter box should be cleaned with warm water and mild detergent
weekly. Allow filter to dry fully before using. Regular cleaning of the gross particulate filter is essential for the safe
operation of the device.
The inlet filter located inside the filter box isdesigned to last up to 2 years depending on the environment. Consult
your equipment provider for further instructions on filter replacement.
Disposal of Equipment and Accessories
Follow your local governing ordinances for disposal and recycling of the OxyHome Oxygen Concentrator and
accessories. IfWEEE regulations apply, do not dispose of unsorted municipal waste. Within Europe, contact the
EU Authorized Representative for disposal instructions.

12
Troubleshooting
If your concentrator fails to operate properly, consult your Equipment Provider, and refer to the troubleshooting
chart below for probable causes and solutions.
Problem Probable Cause Solution
No or low oxygen Internal leak, kinked
cannula, or supply tube. Check supply tube and cannula for obstructions.
Overheating of the device Operating temperature is
too high.
Make sure unit is placed in well-ventilated area and
ventilation ports are not blocked
Ventilation ports are
blocked. Environmental
temperature is too high.
Condensation in supply
tubing and cannula. The device is running hot
which can cause
condensation in the
supply tube and cannula.
Move unit to a well-ventilated area and keep
supply
tubing off cold surfaces.
Cooling fan has
malfunctioned causing the
unit to run hot
Consult your Equipment Provider for service.
Device will not turn on No power to AC outlet Check AC outlet and circuit breaker
Alarm Occurs See alarm indicators Check the indicator lights and LCD display
for details on the alarm. Call your Equipment
Provider for service if necessary.
Product Specifications
Flow Specifications 0 LPM - 5 LPM
Oxygen Concentration 93% (+3%, -3%) (V/V)
Oxygen Output Pressure 8(+2, -2)psi
Rated Voltage/Frequency 120 VAC ±10% 60Hz
Power Consumption 350 watts
Sound ≤45 dB(A)
Dimensions 13.4 in. W x 11.8 in. D x 25.6 in. H
(34 cm x 30 cm x 65 cm)
Weight 41.8Ibs (19kg)

13
The permissible environmental conditions for
transport and storage:
Temperature: -4F to 140F
Humidity limitation: up to 80% RH
Environmental conditions of transport and
storage between uses
Temperature: -13F to 158F
Humidity limitation: ≤90% RH
Humidity limitation:15%RH to 90% RH
Environmental
Operational altitude of concentrator: 0-10,000 ft (3,000 m). When operating the device beyond this altitude range,
it will cause insufficient oxygen concentration.
EMC Information
WARNING: Avoid stacking the device on top or below other electronic equipment. If such use is necessary,
this equipment and the other equipment should be observed to verify that they are operating normally.
WARNING: Use of accessories, transducers, and cables other than those specified or provided by the
manufacturer could result in increased electromagnetic emissions or decreased electromagnetic resistance of this
device and result in malfunction.
WARNING: Portable RF communications equipment (including peripherals such as antenna cables and
external antennas) should not be placed closer than 12 inches (30 cm) to any part of the concentrator.
Table 1
Guidance and Manufacturer’s Declaration: Electromagnetic Emissions
1400-5100 is intended for use in the electromagnetic environment specified below. The customer or the user of 1400-5100 should
assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - Guidance
RF emissions
CISPR11
Group1 1400-5100 uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF emissions
CISPR11
Class B 1400-5100 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

14
Table 2
Guidance and Manufacturer’s Declaration: Electromagnetic Immunity
1400-5100 is intended for use in the electromagnetic environment specified below. The user of 1400-5100 should assure
that it is used in such an environment.
Immunity test IEC 60601 test level
Compliance level
Electromagnetic environment guidance
Electrostatic
Discharge (ESD)
IEC 61000-4-2
±8kV contact
±2kV, ±4kV, ±8kV, ±15kVair
±8kV contact
±2kv, ±4kV, ±8kV
±15kV 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
IEC 61000-4-4
±2kV for power supply lines
±1kV for input/output lines
± 2kV for power
supply lines
±1kV for input/output
lines
The power supply should be that of a
typical
commercial or hospital environment.
Surge
IEC 61000-4-5
±0.5kV, ±1kV line(s) to lines
±0.5kV, ±1kV, ±2kV line(s) to
earth
±0.5kV, ±1kV line(s) to
lines
±0.5kV, ±1kV, ±2kV
line(s) to earth
The power supply 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
0% UT; 0.5 cycle at 0°, 45°,
90°, 135°, 180°, 225°, 270°
and 315°
0%UT;1cycleand
70% UT; 25/30 cycles
Single phase:at0°
0%UT;250/300 cycles
0% U
T
; 0.5 cycle
At 0°,45°, 90°,135°,
180°,225°,270°and
315°
0%UT; 1 cycle
and 70% UT;
25/30 cycles
Single phase: at 0 °
0%UT;250/300 cycles
The power
supply should be that of a typical
commercial
or hospital environment. If
the
user of the 1400-5100 requires
continued
operation during a power
outage
, it is recommended that the
1400
-5100 be powered from an
uninterruptible
power supply or a
battery
Power frequency
(50/60 Hz) magnetic
field
IEC 61000-4-8
30 A/m 30 A/m Power frequency magnetic fields should
be at levels characteristic of a typical
location in a typical commercial or
hospital environment.
NOTE: UTis the a.c. mains voltage prior to application of the test level.

15
Table 3
Guidance and Manufacturer’s Declaration: Electromagnetic Immunity
1400-5100 is intended for use in the electromagnetic environment specified below. The customer or the user of 1400-5100
should assure that it is used in such an environment.
Immunity test IEC 60601 Test Level Compliance level Electromagnetic Environment - Guidance
Conducted RF
IEC 61000
-4-6
3V
0.15 MHz to 80 MHz
6 V in ISM and
3V
0.15 MHz to 80
MHz
6 V in ISM and
amateur radio
bands between
0.15 MHz and
80 MHz
Portable and mobile RF communications equipment should be
used no closer to any part of the device than the recommended
separation distance calculated from the equation applicable to
the frequency of the transmitter.
Recommended separation distance:
150KHz to 80 MHz
80 MHz to 800MHz
80 MHz to 2.7 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, should be less than the compliance
level in each high frequency range.
Interference may occur in the vicinity of equipment marked with
the following symbol:
amateu
r
betwee
n and
80
radio
0.15
MHz
band
s
M
Hz
Radiated RF
IEC61000-4-3
10V/m
80 MHz to 2.7 GHz
10V/m
NOTE 1: At 80MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects, and people.
Field strengths from fixed RF 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 1400-5100 is used exceeds the applicable RF compliance level
above, 1400-5100 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 0.15 MHz to 80 MHz, field strengths should be less than 3 V/m.

16
Table 4
Recommended Separation Distances between Portable and Mobile RF Communications Equipment and this Device
1400-5100 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or
the
user of 1400-5100 can help prevent electromagnetic interference by maintaining a minimum distance between portable and
mobile
RF communications equipment(transmitters)and 1400-5100, as recommended below, according to the maximum output
power
of the communications equipment.
Rated Maximum Output Power
of Transmitter
(W)
Separation Distance According to Frequency of Transmitter
(M)
0.15 MHz to 80 MHz
d=1.2√P
80 MHz to 800 MHz
d=1.2√P
80MHz to 2.7 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.
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects, and people.
Table 5
Declaration - Immunity to proximity fields from RF wireless communications equipment
1400-5100 is intended for use in an electromagnetic environment in which RF wireless communications equipment are controlled.
Immunity
test
IEC60601testlevel Compliance
level
Electromagnetic
environment guidance
Test
frequency
Modulation Maximum
power
Immunity
level
Radiated RF
IEC
61000-4-3
385 MHz **Pulse
Modulation:
18Hz
1.8W 27V/m 27V/m
450 MHz *FM+ 5Hz
deviation:1kHz
sine
2W 28 V/m 28 V/m
710 MHz
745 MHz
780 MHz
**Pulse
Modulation:
217Hz
0.2W 9 V/m 9 V/m

17
810 MHz
870 MHz
930 MHz
**Pulse
Modulation:
18Hz
2W 28 V/m 28 V/m
1720 MHz
1845 MHz
1970 MHz
**Pulse
Modulation:
217Hz
2W 28 V/m 28 V/m
2450 MHz **Pulse
Modulation:
217Hz
2W 28 V/m 28 V/m
5240 MHz
5500 MHz
5785 MHz
**Pulse
Modulation:
217Hz
0.2W 9 V/m 9 V/m
Note *- As an alternative to FM modulation, 50% pulse modulation at 18Hz may be used because while it does not represent
actual modulation, it would be worst case.
Note**-The carrier shall be modulated using a 50% duty cycle square wave signal.
TERMS AND CONDITIONS
1. This warranty is limited to the original purchaser of the unit and is valid for a period of 3 years from the date of
purchase.
2. Any defective part or assembly will be repaired or replaced at the sole discretion and determination of supplier,
if the unit has been properly operated and used during the warranty period.
3. Repairs or replacements of parts under warranty will be carried out by the company or by our approved service
dealers only.
4. Normal maintenance items and disposable components like Cannula, Humidity Bottle, filters etc. are not
covered by this warranty. All expenses incurred in shipping or collecting the unit or its parts, to and from the
company/approved service dealer shall be paid by the purchaser.
5. This warranty does not apply to damages caused by the user or if the device is tampered with, modified, or if
an attempt is made to repair partially/fully by any unauthorized person/party.
6. This warranty will be null and void if the serial number on this product has been altered or removed/or if the
purchaser fails to present the filled warranty card/Manual with which the item was purchased initially.
7. This warranty is null and void if the device is used with dirty/occluded filters or water damage to the electronics
of the machine due to any type of negligence.
8. The customer is responsible for the supply of adequate stabilizer/UPS and input power for the machine. Any
damages caused due to improper power supply voids the warranty.
9. Machine should be run in a clean environment where the dust is minimal.
10.The warranty extended is in lieu of any other express warranties or implied conditions and warranties under
the law and is confined to repairs OR replacement of the defective parts only and does not cover any other direct,
indirect, or consequential losses, which are expressly disclaimed. Furthermore, this warranty in no case shall
extend to payment of any monetary consideration or replacement or return of the product. EXCEPT AS
PROVIDED HEREIN, OXYGO HQ FLORIDA, LLC MAKES NO WARRANTY WHATSOEVER WITH RESPECT

18
TO THE GOODS, INCLUDING ANY (A) WARRANTY OF MERCHANTABILITY OR(B) FITNESS FOR A
PARTICULAR PURPOSE, WHETHER EXPRESS OR IMPLIED BY LAW, COURSE OF DEALING, COURSE OF
PERFORMANCE, USAGE OF TRADE OR OTHERWISE.
Trademarks and Disclaimer
Trademark
All trademarks are the property of their respective owners.
Disclaimer
The information in this document has been carefully examined and is believed to be reliable. Furthermore, the
manufacturer reserves the right to make changes to any products herein to improve readability, function, or
design. The manufacturer does not assume any liability arising out of the application or use of any product or
circuit described herein; neither does itcover any license under its patent rights nor the rights of others.
This Document
The information in this document issubject to change without notice. This document contains proprietary
information that isprotected by copyright. No part of this document may be reproduced in any manner, in whole or
in part (except for brief excerpts in reviews and scientific papers), without the prior written consent of the
manufacturer. Be sure to read carefully and understand all manuals provided with the product.
For Help
If you have questions about the information inthese instructions or about the safe operation of this device, contact
your home oxygen provider or distributor.
To view the most up-to-date version of this manual, please visit our website at www.oxygo.life/oxyhome.
Manufactured for: OxyGo HQ Florida, LLC
2200 Principal Row
Orlando, FL 32837
United States
M544-0623 V15 1170-5400