AirSep® is a registered trademark of AirSep Corporation.
NewLife® Elite and NewLife® are registered trademarks of AirSep Corporation.
MN105-1 Rev. C 02/14
AirSep® Corporation
®
NewLife
Elite Service Manual
Table of Contents
Section 1.0
Introduction
1.1 Equipment Provider Responsibility 1-1
1.2 Important Notice and Symbol Explanations 1-2
1.3 Functional Specications 1-4
Section 2.0
Operation Check
and Oxygen
Concentration Test
2.1 Description of Operation 2-1
2.2 Operation Check 2-1
2.3 Alarm System 2-2
2.3.1 Battery Test 2-2
2.3.2 Power Failure Alarm Test 2-2
2.4 Oxygen Concentration Test and Specication 2-3
Section 3.0
Patient Instructions
3.1 General Instructions 3-1
3.2 Routine Maintenance by the Patient 3-1
3.2.1 Cleaning the Air Intake
Gross Particle Filter 3-1
3.2.2 Checking the Alarm System Battery 3-2
Section 4.0
Equipment Provider
Maintenance
4.1 Routine Maintenance 4-1
4.1.1 Air Intake Gross Particle Filter/GPF 4-1
4.1.2 Product Filter Replacement 4-1
4.1.3 Optional Filter Replacement 4-2
4.1.4 Battery Replacement 4-2
4.1.5 Recording Maintenance 4-3
4.2 Cleaning and Infection Control 4-3
4.2.1 Preparing for New Patient Use 4-4
AirSep® Corporation
i – table of contents
®
NewLife
Elite Service Manual
Section 5.0
Service
5.1 Components 5-1
5.2 Cabinet Removal 5-1
5.2.1 Removing Side Panel(s) 5-1
5.2.2 Removing Back Panel 5-1
5.2.3 Removing Lower Front Cover 5-1
5.2.4 Removing Control Panel 5-1
5.2.5 Superstructure 5-1
5.2.6 Caster Replacement 5-2
5.3 Compressor 5-2
5.3.1 Compressor Replacement 5-3
5.3.2 Capacitor Replacement 5-4
5.4 Solenoid Valves 5-4
5.4.1 Feed or Waste Valve Rebuilding 5-4
5.4.2 Feed or Waste Valve Reassembly 5-5
5.4.3 Solenoid Valve Coil Replacement 5-5
5.5 Sieve Bed Replacement 5-6
5.5.1 Sieve Bed Removal 5-6
5.5.2 Sieve Bed Installation 5-7
5.6 Cabinet Fan Replacement 5-7
5.7 Circuit Board Replacement 5-8
5.7.1 Circuit Board Removal 5-8
5.7.2 Circuit Board Installation 5-9
5.8 Product Regulator Check and Setting 5-10
5.8.1 Setting Product Regulator for
Normal Operation 5-10
5.8.2 Product Regulator Lockout 5-10
5.8.3 Back Pressure Correction at 5 lpm 5-11
5.8.4 Product Regulator Cleaning or
Rebuilding 5-12
5.9 High or Low Pressure Switch Replacement
(In Equipped Units) 5-13
5.10 Circuit Breaker Replacement 5-14
5.10.1 Circuit Breaker Removal 5-14
5.10.2 Circuit Breaker Installation 5-14
5.11 ON/OFF Power Switch Replacement 5-14
5.11.1 ON/OFF Power Switch Removal 5-14
ii – table of contents
AirSep® Corporation
®
NewLife
5.11.2 ON/OFF Power Switch Installation 5-15
5.12 Buzzer Replacement 5-15
5.13 Hour Meter Replacement 5-15
5.14 Flowmeter Replacement 5-16
5.14.1 Flowmeter Removal 5-16
5.14.2 Flowmeter Installation 5-16
5.15 Power Cord Replacement 5-16
Elite Service Manual
Section 6.0
Troubleshooting
6.1 Operating Pressure Test 6-1
6.1.1 High Operating Pressure 6-1
6.1.2 Low Operating Pressure 6-2
6.2 General Troubleshooting 6-2
6.3 Troubleshooting Chart 6-4
6.4 Tool Kit and Pressure Test Gauge 6-7
Appendix
Exploded
Drawings
Figure 2: Main Structure Assembly A-2
Figure 3: Base and Cabinet Components A-3
Figure 4: Test Block Assembly A-4
Figure 5: Valve Block Assembly A-5
Figure 6: Compressor Assembly A-6
Figure 7: Adsorption Bed Assembly A-7
Figure 1: Control Panel Assembly A-1
AirSep® Corporation
iii – table of contents
1.0 Introduction
1.1 Equipment Provider Responsibility
All Equipment Providers of the NewLife® Elite/NewLife® Oxygen Concentrator
must assume responsibilities for handling, operational check-out, patient
instruction, and maintenance. These responsibilities are outlined below and
throughout this manual.
NewLife
®
Elite Service Manual
As an Equipment Provider, you must do all of the following:
Inspect the condition of each NewLife unit immediately upon
delivery to your business location. Note any sign of damage, external
or internal, on the delivery receipt, and report it directly to both the
freight company and AirSep Corporation immediately.
Check the operation of each NewLife before delivery to a patient.
Always operate the unit for a reasonable length of time and check that
the oxygen concentration level is within specications as referred to in
Section 2.4. (Test the battery and power disconnect alarm as described
in Section 2.3 of this manual.)
Deliver NewLife units only to patients authorized by a physician’s
prescription. The NewLife must not be used as a life-supporting
device. A backup supply of oxygen must be available.
Instruct patients how to use the NewLife in conjunction with the
Patient Manual.
Instruct patients to notify their physicians and/or Equipment
Providers if they experience any signs of discomfort.
Instruct each patient how to perform routine maintenance of the air
intake gross particle lter and how to check the alarm system battery.
(Refer to Section 3.2.)
Be available to service each patient at any time.
Maintain the NewLife in accordance with Section 4.0.
Repair components and replace parts only as outlined in this
manual. Use only AirSep parts for replacement in NewLife Oxygen
Concentrators.
WARNING
NewLife units must not be used for or with any lifesupporting applications. Geriatric, pediatric, or any other
patients unable to communicate discomfort while using
this machine may re quire additional monitoring. Advise
patients to immediately notify their Equipment Providers
and/or physicians in case of an alarm or any discomfort.
AirSep® Corporation
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NewLife
®
Elite Service Manual
1.2 Important Notice and Symbol Explanations
As you read the manual, pay special attention to the WARNING, CAUTION, and
NOTE messages. They identify safety guidelines or other important information
as follows:
WARNING:Describes a hazard or unsafe practice that can result in
severe bodily injury or death.
CAUTION:Describes a hazard or unsafe practice that can result in
minor bodily injury or property damage.
NOTE:Provides information important enough to em phasize or
repeat.
1-2
AirSep® Corporation
®
NewLife
Elite Service Manual
The following harmonized symbols (pictograms), used for nonEnglish language countries, will be located on the exterior of
the NewLife unit:
Read the Patient Instruction Manual.
No smoking within ve feet of this device, oxygen-
carrying tubing, or accessories.
No open ames within ve feet of this device, oxygen-
carrying tubing, or accessories.
No oil, grease or petroleum-based products on or near
the unit.
Oxygen outlet
Oxygen alarm
Nebulizer option
AirSep® Corporation
1-3
NewLife
®
Elite Service Manual
1.3FunctionalSpecications
Dimensions:28.5 in. high, 15.7 in. wide, 14.5 in. deep
Concentration:1–3 liters per minute at 95% + 0.5/ - 3%
4 liters per minute at 92% + 3.5/ - 3%
5 liters per minute at 90% + 5.5/ - 3%
Response Time: Allow 5 minutes to attain maximum oxygen
concentration.
Positioning:
0459
Operate the unit in an upright position, maintaining
at least six inches of open space on all sides for
ventilation.
1-4
AirSep® Corporation
®
NewLife
Elite Service Manual
2.0 Operation Check and Oxygen Concentration Test
2.1 Description of Operation
Air enters the NewLife Oxygen Concentrator through an external air intake
gross particulate lter. This ltered air enters the compressor via a suction
resonator, which quiets the compressor’s suction sound. Pressurized air then
exits the compressor and passes through a heat exchanger. The heat exchanger
reduces the temperature of the com pressed air. Next, a two-way solenoid
feed valve directs the air into one of two sieve beds that contain molecular
sieve. The unique property of molecular sieve enables it to physically attract
(adsorb) nitrogen when air passes through this material, thus producing high
concentration oxygen.
There are two sieve beds: while one produces high concentration oxygen, the
other is purged of the nitrogen it adsorbed (collected) while it made oxygen.
Each adsorber produces oxygen for approximately eight seconds and delivers it
to the product tank. Oxygen exits the product tank through a pressure regulator,
product lter, ow control valve, owmeter, and nally exits the unit. The ow
control valve, which is part of the owmeter, controls the amount of oxygen
delivered to the patient. The NewLife unit delivers up to 95.5% pure oxygen at
ow rates from 1–5 lpm.
NOTE: NewLife Elite OxiSilent™ option incorporates an additional felt intake
lter prior to air entering the compressor.
2.2 Operation Check
AirSep tests every NewLife Oxygen Concentrator thoroughly after manufac-
ture. You must perform the following test to ensure that no damage occurred
in shipping or handling.
1 Open and inspect all cartons (that contain units) upon delivery. Unpack
the unit and remove it from the carton. Inspect the unit itself for
damage. If the exterior of a unit’s carton is damaged, or the unit itself
is damaged, note it on the freight bill signed by the driver.
2 Plug in the power cord of the unit, and set the ON/OFF switch to the
ON position. Check to see that the following occurs:
a. A continuous alarm loudly sounds for approximately
ve seconds to indicate that the battery for the alarm
is good. See the trou bleshooting chart in Section 6.0 of
this manual if the unit’s alarm does anything other than
sound loudly for ve seconds.
AirSep® Corporation
b. The compressor runs. Listen for the sound.
c. Exhaust air ows out of the bottom of the unit.
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NewLife
®
Elite Service Manual
d. OPTIONAL: The Oxygen Monitor’s amber light
remains on until the oxygen concentration reaches 85%
± 3% (approximately two minutes).
3 Turn the owmeter adjustment knob counterclockwise until it stops
(wide open).
The maximum ow should register 5.5 lpm (the 5.5 lpm line should
appear to split the middle of the owmeter ball) with no connections
at the oxygen outlet. If not, refer to Section 5.8.1 to set the product
regulator.
4 Perform an oxygen concentration test, as described in Section 2.4.
2.3 Alarm System
The NewLife Oxygen Concentrator is equipped with a battery-powered alarm
system, which sounds a continuous and loud alarm when a power failure
occurs. It sounds an intermittent alarm if the high or low pressure indicators
are activated or if the optional oxygen monitor detects lower than therapeutic
levels of oxygen concentration. The alarm remains on until you correct the alarm
condition or you set the ON/OFF switch to the OFF position. Refer to Section
6.0 for a list of probable alarm causes.
2.3.1 Battery Test
Each time the NewLife unit is turned on, a ve-second audible alarm
sounds to indicate the condition of the battery.
NOTE
The audio alarm must sound loudly for
approximately ve seconds each time the unit is
turned to ON to indicate the bat tery is in good
condition.
2.3.2 Power Failure Alarm Test
To test the power failure alarm, take the following step:
Unplug the unit, and set the ON/ OFF switch to the ON position.
This should immediately activate the audio alarm. If it does not, refer
to the troubleshooting chart in Section 6.0 of this manual.
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AirSep® Corporation
®
NewLife
Elite Service Manual
2.4OxygenConcentrationTestandSpecication
To ensure that the unit’s output of oxygen is within specication, you
must perform a test of oxygen concentration. Test the unit upon delivery
to a patient and at periodic intervals. Equipment Providers, based on
their expertise and documentation, may establish and implement their
own protocol to check oxygen concentration. The interval established
may be longer or shorter than 90 days, which is AirSep’s default time
period for providers who do not choose to establish their own protocol.
1 If an oxygen humidier bottle is used, remove it from the oxygen
outlet.
2 Connect a calibrated oxygen concentration analyzer to the oxygen
outlet.
3 Verify that the product ow rate delivered by the unit matches the
patient’s prescription and does not exceed the capacity of the unit.
4 Set the unit’s ON/OFF power switch to the ON position. (It takes
approximately five minutes for the oxygen concentration to
stabilize.) Take oxygen concentration readings every 60 seconds
until the analyzer shows that two consecutive readings are the
same.
5 Disconnect the oxygen analyzer, and reconnect the humidier
bottle (if used) and any other equipment/ accessories that may be
required.
6 Adjust the owmeter adjustment knob to the prescribed level.
NOTE
Do not measure oxygen concentration output
after the product stream passes through a
humidier bottle, or erroneous readings will
result.
AirSep NewLife Oxygen Concentration Specications
Liter Flow SpecicationIn Spec
1–3 lpm 95% + 0.5/ - 3% 92% or higher
4 lpm 92% + 3.5/ - 3% 89% or higher
AirSep® Corporation
5 lpm 90% + 5.5/ - 3% 87% or higher
2-3
®
NewLife
Elite Service Manual
3.0 Patient Instructions
3.1 General Instructions
It is important that patients thoroughly understand how to operate the AirSep
NewLife unit. This enables proper treatment as prescribed by a qualied,
licensed physician. You must explain that the purpose of this therapy is to
alleviate symptoms. If patients experience any discomfort or the unit alarms,
they must notify their Equipment Provider and/or physician immediately.
You, as the Equipment Provider, are responsible to see that each patient receives
the Patient Manual. Locate the Patient Manual in the pocket on the back of each
unit. Explain each step in the operation of the unit to the patient in reference to
this manual.
3.2 Routine Maintenance by the Patient
To ensure accurate output and efcient operation of the unit, the patient must
perform two simple routine maintenance tasks:
Clean the air intake gross particle lter
Check the alarm system battery
3.2.1 Cleaning the Air Intake Gross Particle Filter
NOTE
The patient must clean this lter weekly, as
described below. The lter may require daily
cleaning if the NewLife unit operates in a harsh
environment such as a house heated by wood,
kerosene, or oil, or one with excessive cigarette
smoke.
1 Remove the dirty air intake gross particle lter from the back
of the NewLife unit, and install the clean lter stored in the
pocket on the back of the unit.
2 Wash the dirty lter in warm soapy water, and rinse.
3-1
3Use a soft absorbent towel to remove excess water.
4 Place the clean air intake gross particle lter in the pocket on
the back of the unit.
AirSep® Corporation
®
NewLife
Elite Service Manual
3.2.2 Checking the Alarm System Battery
The alarm system battery is tested each time the ON/OFF switch is
set to the ON position. A continuous alarm sounds for approxi mately
ve seconds to indicate a good battery. If the alarm does anything
other than sound loudly for ve seconds, instruct the patient to call
the Equipment Provider immediately.
AirSep® Corporation
3-2
®
NewLife
Elite Service Manual
4.0 Provider Maintenance
4.1 Routine Maintenance
The NewLife Elite unit has two or three lters and a 9-volt battery that require
sched uled maintenance and replacement.
To ensure that the unit’s output of oxygen is within specication, you must
perform a test of oxygen concentration. Test the unit upon delivery to a patient
and at periodic intervals. Equipment Providers, based on their expertise and
documentation, may establish and implement their own protocol to check
oxygen concentration. The interval established may be longer or shorter than
90 days, which is AirSep’s default time period for providers who do not choose
to establish their own protocol.
AirSep does not require preventative maintenance on the concentrator. You
do not need to perform any maintenance as long as the NewLife unit remains
within specications at the desired ow rate.
4.1.1 Air Intake Gross Particle Filter/GPF
The external air intake gross particle lter is located on the back of the
unit. You can easily remove it by hand. Instruct the patient to clean
this lter weekly. (Refer to Section 3.2.1.)
NOTE
The lter may require more frequent cleaning if
the NewLife unit operates in a harsh environ ment
such as a house heated by wood, kerosene, or oil,
or one with excessive cooking or cigarette smoke.
4.1.2 Product Filter Replacement
The product lter must be replaced after every 25,000 hours of use.
1Set the unit’s ON/OFF switch to the OFF position, and unplug
the power cord.
2 Remove the side panels to locate the product lter.
NOTE
Observe the position of the lter before
removal.
4-1
3Cut the tie-wraps, and separate the green tubing from both
sides of the lter.
AirSep® Corporation
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