5.10.2 Circuit Breaker Installation23
I/0 (ON/OFF) Power Switch Replacement23
5.11.1 I/0 (ON/OFF) Power Switch Removal23
5.11.2 I/0 (ON/OFF) Power Switch Installation24
Buzzer Replacement24
Hour Meter Replacement24
Flow Meter Replacement24
5.14.1 Flow Meter Removal24
5.14.2 Flow Meter Installation24
Power Cord Replacement24
Section 6.0
Troubleshooting
Air Pressure Test (P1)25
6.1.1 High Air Pressure25
6.1.2 Low Air Pressure26
Product Pressure Test (P2)26
6.2.1 High Product Pressure26
6.2.2 Low Product Pressure27
General Troubleshooting27
Troubleshooting Chart28-32
Tool Kit and Pressure Test Gauge33
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Appendices
Exploded
Parts Listing
Maintenance
Drawings
A1: Base Assembly
A1.1: Base Assembly
A2: Main Structure Assembly – Front View36
A3: Main Structure Assembly – Rear View37
A4: Regulator Assembly38
A5: Compressor Assembly
A5.1: Compressor Assembly
A6: Control Panel Assembly; OCSI Unit - Front41
A7: Control Panel Assembly; OCSI Unit - Rear42
A6.1: Control Panel Assembly; OCSI Unit - Front43
A7.1: Control Panel Assembly; OCSI Unit - Rear44
A8: Control Panel Assembly; Non OCSI Unit Front
A9: Control Panel Assembly; Non OCSI Unit –
Rear
A10: Air Tank Assembly47
A10.1: Air Tank Assembly48
A11: Front Cabinet Assembly49
A11.1: Front Cabinet Assembly50
A12: Rear Cabinet Assembly51
A12: Rear Cabinet Assembly52
A13: Module Assembly53
34
35
39
40
45
46
Record
A14: Replacement Parts Listing54-57
A15: Maintenance Log58-59
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Page 6
General Safety Instructions
Production and use of oxygen
Oxygen is not a flammable gas, but accelerates the combustion of materials. To
prevent fire risks, the MARK5 NUVO should be kept away from flames,
incandescent sources or sources of heat (cigarettes) and combustible products
such as oil, grease, solvents, aerosols, etc.
Do not use in an explosive atmosphere.
Prevent oxygen from accumulating on upholstered seats or any other fabric. If the
concentrator operates without being administered to a patient, locate it so that the
flow of gas generated is dissipated into the air.
Locate the equipment in a free space (filter to the rear and below) which is well
ventilated and free of fumes or atmospheric pollution.
Use and Maintenance of the Device
Use the electric cable provided and check that the voltage of the mains socket used
complies with the electrical characteristics of the appliance indicated on the
manufacturers plate on the rear of the appliance.
Do not use an extension cord or multiple sockets which can create sparks and
therefore pose a fire risk.
Use of the MARK5 NUVO must be restricted solely to oxygen therapy on medical
prescription in compliance with the daily rate and duration.
Use in other circumstances may represent a hazard to patient health.
Do not use in a specifically magnetic environment (MRI, etc.).
The MARK5 Nuvo has an audible alarm intended to warn the user of any
problems. The user must determine the maximum distance away from the
Nuvobased on the on the sound levels in the environment, to ensure that the
alarm is always audible.
Standards & Regulations
In compliance with UL60601-1 [EN60601-1] (para 6.82.b):
“The manufacturer, assembler, installer or importer are not considered to be
responsible for consequences or the safety, reliability and characteristics of a
device unless,
● the assembly, extensions, adjustments modifications or repairs have been
performed by persons authorized by the manufacturer,
Page 6 of 592010-2225 Rev - B
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● the electrical installation of the corresponding premises complies with appropriate
regulations and codes,
● the device is used in accordance with the instructions for its use.
If the replacement parts used for periodic servicing by an approved technician do
not comply with the manufacturer’s specifications, the manufacturer is absolved of
all liability in the event of an incident.
Do not open the equipment when it is powered on: risk of electrocution.
This device complies with the requirements of the FDA Quality System Regulation
and EU Directive 93/42/EEC, but its operation may be affected by the use in the
surrounding area of appliances such as diathermy, high frequency electro-surgical
instruments, defibrillators, short wave treatment appliances, cell-phones, CB
devices and other portables, microwave ovens, induction hot plates or remote
control toys, and more generally, by electromagnetic interference exceeding the
levels specified in standard IEC(EN) 60601-1-2.
1.0Introduction
1.1Home Service Provider Responsibility
All HomeServiceProviders oftheNidekMedical Mark5Nuvo®Oxygen
Concentrator must assume responsibilities for handling, operational check-out,
patient instruction, and maintenance. These responsibilities are outlined below and
throughout this manual.
WARNING
Mark5 Nuvo units must not be used for or with any life-supporting or life sustaining
applications.Patients unable to communicate discomfort while using this device
may require additional monitoring. Advise patients to immediately notify their Home
Service Provider(s) and/or physician(s) in case of an alarm or any discomfort.
As a Home Service Provider, you must do all of the following:
● Inspect the condition of each Mark5 Nuvo® 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 Nidek Medical Products, Inc. immediately.
● Check the operation of each Mark5 Nuvo® before delivery to a patient.
Always operate the unit for a reasonable length of time and check that the
oxygen concentration level is within specifications as referred to in
Section 2.4. Test the battery and power disconnect alarm as described in
Section 2.3 of this manual.
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Page 8
● Deliver Mark5 Nuvo® units only to patients authorized by a physician’s
hazard or unsafe practice that can result
Describes a hazard or unsafe practice that can result
Provides information important enough to emphasize
prescription. The Mark5 Nuvo® must not be used as a life-supporting or
life sustaining device. A backup supply of oxygen must be available.
● Instruct patients how to use the Mark5 Nuvo® in conjunction with the
Patient Manual.
● Instruct patients to notify their physicians and/or Home Service Providers
if they experience any signs of discomfort.
● Instruct each patient how to perform routine maintenance of the cabinet
air filter and how to check the alarm system battery. (Refer to Section
3.2.)
Be available to service each patient at any time. Maintain the Mark5
Nuvo® in accordance with Section 4.0.
Repair components and replace parts only as outlined in this manual. Use only
Nidek Medical parts for replacement in Mark5 Nuvo® Oxygen Concentrators.
● Refer to the Mark5 Nuvo® Product Warranty if parts replacement is
required within the warranty period.
1.2Important 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:
CAUTION:
NOTE:
The following harmonized symbols (pictograms), used for non-English language
countries, will be located on the exterior of the Mark5 Nuvo® unit:
Store, ship and use the device in an upright condition.
Describes a
in severe bodily injury or death.
in minor bodily injury or property damage.
or repeat.
No smoking within five feet of this device, oxygen-carrying tubing, or
accessories.
Indicates an alarm signal.
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Do not use any oil or grease on or near the device
1.3Functional Specifications
Dimensions: 15.5 in. long, 15.6 in. wide, 27.8 in. tall
(394 mm long, 396 mm wide, 706 mm high)
Weight:50 to 54 Ib (22.5 to 24.5 kg) depending on sound attenuation;
Electrical120 VAC, 60 Hz, 4 amps, 410 watts
Requirements:220 VAC, 50 Hz, 2 amps, 420 watts
Capacity:5 liters per minute at 90% oxygen
(Based on 70°F [21°C] at sea level)
Accuracy:Flow meter ±5% full scale. (Based on pre-calibrated analysis.)
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:Acceptable concentration is normally achieved in about
90 seconds; allow 5 minutes to attain full concentration.
Positioning:Operate the unit in an upright position, maintaining at
least six inches of open space on all sides for ventilation.
2.0Operational Check and Concentration Test
2.1Description of Operation
Air enters the Mark5 Nuvo® Oxygen Concentrator through an external cooling air
intake filter. This filtered air enters the compressor via a suction resonator and fine
filter, which quiets the suction sounds made by the compressor. Pressurized air
then exits the compressor and passes through a heat exchanger into an air tank.
The heat exchanger reduces the temperature of the compressed air and the air tank
stores air when feed is interrupted. Next, a rotary poppet feed valve directs the air
into one of two sieve beds that contain molecular sieve. The special characteristic
property of molecular sieve is that it physically attracts (adsorbs) nitrogen when air
passes through this material, thus enabling the production of high purity oxygen.
There are two sieve beds or adsorbent columns; while one produces high purity
oxygen, the other is purged of the nitrogen it adsorbed (collected) while it was
producing oxygen. Each column produces oxygen for approximately four seconds
and delivers it to the product storage volume in the end of the column. Oxygen exits
the adsorbent column through a pressure regulator, flow control valve, flow meter,
and final product filter. The flow control valve, which is part of the flow meter,
controls the flow rate of oxygen delivered to the patient. The Mark5 Nuvo® unit
2010-2225 Rev - BPage 9 of 59
Page 10
delivers up to 95% oxygen concentration at flow rates from 1 to 5 l/min.The
remaining constituents of the product gas stream are nitrogen and argon, both of
which are part of the air we breathe, are inert and are completely safe.
2.2Operational Check
Nidek Medical runs each device through a burn in period and tests every Mark5
Nuvo® Oxygen Concentrator thoroughly after manufacture before releasing for
shipment. As the home service provider, it is your responsibility to perform the
following test to ensure that no damage occurred in shipping or handling.
1.Open and inspect all concentrator cartons upon receipt. Unpack each
unit and remove it from its carton. Inspect the unit itself for damage. If
the exterior of the carton is damaged, or the unit itself is damaged,
note it on the freight bill signed by the driver.
● Before plugging the unit into the wall outlet, actuate the I/0
(ON/OFF) switch to the I (ON) position and note that the audible
alarm sounds continuously. (See Section 2.3). Move the switch to
the 0 (OFF) position.
2.Plug in the power cord of the unit, and set the I/0 (ON/OFF) switch to
the I (ON) position. Check to see that the following occurs:
● The compressor runs, listen for the sound.
● Exhaust air flows out of the bottom of the unit.
● OPTIONAL for Units Equipped with Oxygen Concentration Status
Indicator (OCSI): The OCSI green light remains off until the oxygen
concentration reaches 85% ± 3% (82% ± 2% for 50 Hz units)
(approximately two minutes).
3.Turn the flow meter adjustment knob counterclockwise until it stops
(wide open). The flow meter should register in excess of 5.5 liters/min.
If not, refer to Section 5.8 to adjust the product regulator.
4Perform an oxygen concentration test, as described in Section 2.4.
2.3Alarm System
The Mark5 Nuvo® Oxygen Concentrator is equipped with a battery-powered alarm
system, which sounds a continuous and loud alarm when a power failure occurs or
when one or more cycle variables are not within specification. It sounds an alarm if
the high or low pressure indicators are activated or if the optional OCSI detects
lower than predetermined levels of oxygen concentration. The alarm remains on
until you correct the alarm condition or you set the I/0 (ON/OFF) switch to the 0
(OFF) position. Refer to Section 6.0 for a list of probable alarm causes,
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2.3.1 Battery Test
The Mark5 Nuvo® battery can be checked by observing that the continuous alarm
sounds when the I/0 (ON/OFF) switch is moved to the I (ON) position when the unit
is unplugged from the wall outlet.
2.3.2 Power Failure Alarm Test
To test the power failure alarm, perform the following actions:
Unplug the power cord from the wall outlet, and set the I/0 (ON/OFF) switch to the I
(ON) position.
This should immediately activate the audible alarm. If it does not, refer to the
troubleshooting chart in Section 6.0 of this manual.
2.4Oxygen Concentration Test and Specification
To ensure that the output of oxygen from the device is within specification, you must
perform an oxygen concentration test. Test the unit upon delivery to a patient and at
periodicintervals.HomeServiceProviders,basedontheirexpertiseand
documentation, may establish and implement their own plans for checking oxygen
concentration. The interval established may be longer or shorter than 90 days,
which is Nidek Medical’s default time period for providers who do not choose to
establish their own plan.
1.If an oxygen humidifier bottle is used, remove it from the oxygen outlet.
2.Connect a calibrated oxygen concentration analyzer to the oxygen outlet.
3.Set the I/0 (ON/OFF) power switch to the I (ON) position. (It takes
approximately five minutes for the oxygen concentration to stabilize.) Take oxygen
concentration readings over a period of several minutes to reduce any cyclic
variations
4.Verify that the product flow rate delivered by the unit matches the patient’s
prescription and does not exceed the capacity of the unit.
5.Disconnect the oxygen analyzer, and reconnect the humidifier bottle (if used)
and any other equipment / accessories that may be required.
6.Adjust the flow meter adjustment knob to the prescribed flow rate.
NOTE
Do not measure oxygen concentration output after the product stream passes
through a humidifier bottle, erroneous readings will result and your oxygen
concentration measuring device might be damaged.
2010-2225 Rev - BPage 11 of 59
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Nidek Medical Mark5 Nuvo® Concentration Specifications
air filter from the back of the
with household
Reinstall the clean air filter on the grille in the back of
Liter FlowSpecificationWithin Specification
1 to 3 l/min95% + 0.5 / - 3%92% or higher
4 l/min92% + 3.5 / - 3%89% or higher
5 l/min90% + 5.5 / - 3%87% or higher
3.0Patient Instructions
3.1General Instructions
It is important that patients thoroughly understand how to operate the Nidek Medical
Mark5 Nuvo® unit. This enables proper treatment as prescribed by a qualified,
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 Home Service Provider and/or physician immediately.You, as the Home
Service Provider, are responsible to see that each patient receives the Patient
Manual. Explain each step in the operation of the unit to the patient in reference to
this manual.
3.2Routine Maintenance by the Patient
To ensure accurate output and efficient operation of the unit, the patient must
perform two simple routine maintenance tasks:
•Clean the cabinet air filter
•Check the alarm system battery
3.2.1 Cleaning the Cabinet Air Filter
NOTE:
The patient must clean this filter weekly, as described below. The filter
may require daily cleaning if the Mark5 Nuvo® unit operates in a harsh
environment such as a house heated by wood, kerosene, or oil, or one
with excessive cigarette smoke.
1Remove the dirty cabinet
Mark5 Nuvo® unit.
2Wash the dirty filter in warm water
detergent, and rinse.
3Use a soft absorbent towel to remove excess water.
4
the unit.
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3.2.2 Checking the Alarm System Battery
See Procedure described in Paragraph 2.3.1
4.0Home Service Provider Maintenance
4.1Routine Maintenance
The Mark5 Nuvo® unit has two filters and a 9-volt battery that require scheduled
maintenance and replacement.
To ensure that the output of oxygen from the unit is within specification, you must
perform an oxygen concentration test. Test the unit upon delivery to a patient and at
periodicintervals.HomeServiceProviders,basedontheirexpertiseand
documentation, may establish and implement their own practices for checking
oxygen concentration. Consult Nidek Medical’s Service and Maintenance Log (A-
15) for the recommended intervals for testing.
Nidek Medical does not require preventive maintenance on the concentrator. You
do not need to perform any maintenance as long as the Mark5 Nuvo® unit remains
withinspecificationsattheprescribedflowrate.(Refer toSection2.4)
Cabinet Air Filter
The external cabinet air filter is located on the back of the unit, You can easily
remove it by hand. Instruct the patient to clean this filter weekly. (Refer to Section
3.2.1.)
NOTE
The filter may require more frequent cleaning if the Mark5 Nuvo® unit operates in a
harsh environment such as a house heated by wood, kerosene, or oil, or one with
excessive cooking, cigarette smoke or atmospheric dust.
4.1.2 Final Product Filter Replacement
The final product filter does not require periodic replacement; it needs to be
replaced only if it restricts oxygen flow. It is suggested that it be replaced whenever
the sieve module is repaired or replaced and after the compressor is rebuilt.
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the cabinet back to locate the final product filter.
NOTE: Observe the position of the filter before removal.
3.Separate the silicone tubing from both sides of the filter.
4.Install the new filter with the inlet side in the same position as before. Push
the tubing together so that it overlaps the barbs of the final product filter
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connections.
5.Record information about the final product filter replacement in Appendix 15
of this manual and online at www.nidekmedical.com under the ‘Maintenance
Log’ tab.
6.Reinstall the cabinet back.
4.1.3 Inlet Air Filter Replacement
The inlet air filter requires inspection at each patient visit. The filter should be
replaced annually, or more often depending on environment.
1.Set the unit I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the
power cord.
2.Remove the rear cabinet access panel to locate the inlet air filter.
3.Remove filter from the unit, and replace with a new filter.
4.Record information about the filter replacement in Appendix 15 of this
manual and online at www.nidekmedical.com under the ‘Maintenance Log’
tab.
5.Reinstall the access panel.
4.1.4 Battery Replacement
Each time the standard Mark5 Nuvo® unit is turned on, the alarm must sound loudly
for approximately five seconds to indicate a good battery. An alarm that does
anything other than sound loudly for five seconds indicates a weak battery and
requires replacement. For units with OCSI, actuate the switch with the power cord
unplugged to test the battery.
To replace the battery, take the following steps:
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the access panel in the cabinet back.
3.Pull the battery from the mounting slot and remove the connection wires.
4.Attach the new battery to the connector and reinsert it into the mounting slot.
5.Set the I/0 (ON/OFF) switch to the I (ON) position to test the alarm.
6.Record the battery replacement information in Appendix 15 of this manual
and online at www.nidekmedical.com under the ‘Maintenance Log’ tab.
7.Reinstall the access panel.
4.1.5 Wick Replacement
The wick is installed in the process air stream of the unit, connected to the air tank,
to assist with removal of moisture from the air.This helps prevent premature
contamination of the sieve beds, particularly in humid climates. The wick should be
replaced at each compressor service / module replacement; it is suggested that
more frequent replacement be done in very humid climates. The wick is located in
a bushing located just to the right of the gearmotor. It is installed in a quick release
fitting. Pull the fitting from the bushing by hand – it may require several pounds of
force, remove the wick and install a new one in its place. Re-insert the wick end
and fitting into the bushing so the wick is totally below the base plate surface.
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4.1.6 Recording Maintenance
As the Home Service Provider, it is suggested that you record all routine
maintenance and repairs performed on the Mark5 Nuvo® unit, including hours and
dates of service in Appendix 15 of this manual and online at www.nidekmedical.com
under the ‘Maintenance Log’ tab.
4.2Cleaning and Infection Control
With the growing concern about possible cross infection from home oxygen
equipment (i.e.. oxygen concentrators) from one home care patient to another,
appropriate cautions should be exercised.
The organisms of most concern are M. Tuberculosis, HIV, and Viral Hepatitis.
These are potentially pathogenic.
Tuberculosis can survive outside of the human body, but its mode of transmission is
by droplet nuclei. When infected individuals cough, they release droplet nuclei into
the air, and these carry the Tuberculosis organism. Another person may breathe in
these droplet nuclei, but prolonged exposure to the infected person is usually
necessary for infection to occur.
HIV and Viral Hepatitis are both viruses, which are not living cells themselves but
which can duplicate when in a living “host” cell. Both of these organisms are usually
passed on by person-to-person contact, and both need to be in the human body to
survive. Once outside the body, viruses can survive for only a short period of time.
4.2.1 Preparing for New Patient Use
When you remove the Mark5 Nuvo® from a patient’s home, always dispose of the
used nasal cannula and humidifier bottle. Clean the exterior of the Mark5 Nuvo®
with a soapy water solution or commercial detergent cleaner to remove any gross
debris, organic or otherwise. Be careful not to get any liquid into the interior of the
unit.
Next, clean the exterior with either a common chemical disinfectant or a bleach
solution* and allow it to air dry.For the bleach solution, wear eye and skin
protection to prevent exposure to the chlorine. Retest the Mark5 Nuvo® before you
return it to your inventory.
Replace the cabinet air filter between each patient’s use or clean with warm soapy
water if it is in good condition. Clean this filter at least once per week or more
frequently if operated in a dusty environment.
*Make the bleach solution a 1:100 dilution of 5.25% sodium hypochlorite. Mix one
part household bleach (e.g. Clorox) with 99 parts cold tap water. To measure the
2010-2225 Rev - BPage 15 of 59
Page 16
solution easily, take 1/4 cup of household bleach, and mix it with a gallon of cold tap
water. Allow the mixture to sit on potentially contaminated surfaces for 10 minutes.
5.0 Service
5.1Components
The design of the Nidek Medical Mark5 Nuvo® Oxygen Concentrator allows for
easy access and removal of most components. This allows you to perform
scheduled maintenance, repair, and replacement of parts with minimal time and
effort.The inlet air filter and battery are conveniently located inside the small
access panel in the cabinet back.
CAUTION:
For your safety, be sure to set the I/0 (ON/OFF) switch to the 0 (OFF)
position and unplug the power cord before you service the Mark5 Nuvo®
Oxygen Concentrator.
NOTE: Record all scheduled maintenance. (Refer to Section 4.1.6.)
5.2Cabinet Removal
5.2.1 Removing Cabinet Back
To remove the cabinet back, remove two screws near the base (one on each side)
and two inset screws at the top just under the handle.
5.2.2 Removing Cabinet Front
To remove the cabinet front, remove two screws near the base (one on each side)
adjacent to the rear cabinet screws and two inset screws at the top just under the
handle. It is necessary to remove the cabinet back to access the top screws.
5.2.3 Removing Control Panel
Eight screws hold the control panel in place; the front cover must be removed to
access these screws. It is necessary to remove the electrical wiring and pneumatic
tubing to fully release the control panel.
5.2.4 Main Structure
The weight and forces of the internal components rest solely on four parts: the main
structure, the compressor plate, the base-plate and the base. These parts were
specially designed and formed. They should never require replacement under
normal use.
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5.2.5 Caster Replacement
The casters are a push in type that does not require any fastener. Lay the device
on its back to access the casters from the bottom. Pull them straight out away from
the bottom.
5.3Compressor
The compressor is the pump within the oxygen concentrator that supplies air to the
separation process performed by the sieve beds. The pressure generated by the
compressor forces oxygen to flow out of the top of the sieve columns.
The compressor is the likely cause of two potential specific problems:
a. An insufficient amount of air is supplied to the process, and
b. An excessive sound level.
● Air Supply
Compressor output refers to how much compressed air the compressor can
produce. This depends upon the model of the compressor, length of stroke, piston
diameter, speed of rotation and condition of seals. The cup seals form the seal
between the piston and the cylinder wall. As the cup seals wear, the output begins
to gradually decrease. This reduction in compressor output results in less air, and
thus less oxygen, entering the sieve beds. Therefore, the production of oxygen
decreases.
Because this drop in oxygen production occurs over a long period of time,
preventive maintenance on the compressor is not required.
You can continue a patient’s therapy on the Mark5 Nuvo® unit as long as the
oxygen concentration level at the prescribed liter flow rate is within Nidek Medical’s
specification limits. Refer to Section 2.4.
The sound level is largely determined by the condition of the compressor’s
bearings.
There are four bearings located within the compressor that allow the inner
components of the compressor to rotate. If the bearings wear to the point that they
become loose and noisy, the compressor becomes noticeably loud and needs
servicing. The life of a compressor is determined primarily by its operating
temperature. It is extremely important that the cabinet air filters are cleaned and
replaced as required.
5.3.1 Compressor Replacement
Remove Compressor Assembly
To remove the compressor assembly for exchange, follow the steps listed below:
1.Set the unit’s I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the
power cord.
2.Remove the cabinet back and front.
3.Disconnect the suction tube.
4.Disconnect the two compressor power cable leads and the two leads to the
capacitor at the inline connector.
5.Remove the three screws that connect the compressor plate to the base of
the unit, lift and slide out the compressor assembly.
6.Remove compressor from the plate by removing the four compressor bolts.
7.Remove tie wrap from compressor plate wiring harness.
8.Remove the heat exchanger tubing and fittings.
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Compressor Assembly Installation
To install the rebuilt compressor assembly, follow the steps listed below:
1.Perform the compressor removal procedure in reverse order.
2.Leak test all connections.
5.3.2 Capacitor Replacement
The capacitor helps the compressor to start and run more efficiently. If the
compressor cannot start, the capacitor may be defective and require replacement.
Thecapacitorshouldbereplacedateachcompressorservice/module
replacement. To replace the capacitor, take the following steps:
1.Set the unit’s I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug
the power cord.
2.Remove the rear and front cabinets.
3.Disconnect the two leads to the capacitor and remove the nut from the
mounting screw.
4.Remove the nut and washer below the capacitor.
5.To install the new capacitor, connect the leads and replace the capacitor and
associated hardware.
5.4Process Control Valve
The Mark5 Nuvo® uses a gearmotor powered rotary cam-operated poppet valve
assembly to control the air separation process. There is a feed port that connects
to the air tank and an exhaust port that connects to the exhaust muffler. There are
three possible valve states as follows:
1.Air feed connected to sieve bed A and exhaust connected to sieve bed B.
2.Air feed connected to sieve bed B and exhaust connected to sieve bed A.
3.Both ports closed; this is a very short time period during which air pressure
builds in the air tank.
The control valve of the Mark5 Nuvo® unit requires no scheduled maintenance. If a
valve does not function as required, it is best to replace the complete sieve module
as it is probable that one or both of the beds has been damaged.
5.5Sieve Bed Replacement
CAUTION:
Do not expose molecular sieve (contents of bed) to air for an extended period of
time. Prolonged exposure of molecular sieve to the moisture in room air results in
contamination and permanent damage to the sieve material. Keep all openings to
the sieve beds sealed during periods of storage.
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NOTE
If replacement is necessary, you must replace both sieve beds at the same time. It
is recommended to replace the sieve beds and control valve module as a complete
assembly.
5.5.1 Sieve Bed Removal
1.Set the unit’s I/0 (ON/OFF) switch to the 0 (OFF) position and unplug the
power cord.
2.Remove the cabinet back.
3.Disconnect the 1/4-inch product tube from the top of one of the beds.
4.Remove the 4 tie-wraps ( 2 from each sieve bed ). Note their position and
orientation.
5.Remove two “Z” brackets; one from the top of each of the sieve beds.
6.Lift the module up and out of the base plate cradle.
7.Unplug the valve gearmotor electrical leads at the in-line connections.
8.Manipulate the module so that the black exhaust hose can be removed from
the fitting on the valve.
9.Loosen the hose clamp and remove the black feed hose from the fitting on
the valve.
5.5.2 Sieve Bed Installation
To install the sieve beds, follow the sieve bed removal procedure in reverse order. It
is very important to tighten all tubes to eliminate leaks. However, do not over
tighten.
To check for leaks, take the following steps:
1.Plug in the unit.
2.Set the unit’s I/0 (ON/OFF) switch to I (ON) for three minutes with the
flowmeter closed to pressurize the system.
3.Apply soapy water around the hose connections at the valve and the
air tank; check for leaks.
Caution: There is an electrical shock hazard with the Power ON. Be
careful that no water contacts any of the electrical connections.
NOTE
Even small leaks can affect concentrator performance and can cause contamination
of the sieve. Careful leak testing is important.
5.6Cabinet Fan Replacement
The cabinet fan for the Mark5 Nuvo® is located under the compressor. Refer to the
troubleshooting chart in Section 6.0 of this manual for instances where replacement
of the fan may be required.
To replace the cabinet fan in the Mark5 Nuvo® unit, take the following steps:
1.Set the unit’s I/0 (ON/OFF) switch to the 0 (OFF) position and unplug the
Page 20 of 592010-2225 Rev - B
Page 21
power cord.
2.Remove the front and back cabinets.
3.Follow the procedure in 5.3.1 to remove the compressor assembly.
4.Disconnect the fan leads.
5.Position the new cabinet fan so that the air flow arrow points toward the
bottom and the electrical connections.Be sure that the electrical wires do
not interfere with the rotation of the fan.
6.Connect the fan leads and place the fan on the mounting pins.
7.Replace compressor assembly.
8.Reinstall the front and back cabinets.
5.7Circuit Board Replacement
The printed circuit board controls the alarm system functions.
Consult the troubleshooting chart in Section 6.0 to determine when to replace the
printed circuit board.
CAUTION
The Printed Circuit Board (PCB) contain components that are sensitive to
electrostatic discharge (ESD) that can damage the board if not handled properly. As
when handling any ESD sensitive PCB, observe standard ESD safety procedures.
These procedures include the following:
• Handle the PCB by the edges only.
• Work on a grounded ESD mat.
• Wear a grounded wrist strap.
• Store PCB in anti-static bags only.
5.7.1 Circuit Board Removal (Note that the Circuit Board on the OCSI unit is
different to the Circuit Board on the standard unit.)
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the front and cabinet backs.
3.Remove the control panel to which the circuit board is attached.
4.Disconnect the 7-pin connector from the circuit board.
5.Disconnect tubing from each end of the black sensor tube on the OCSI unit,
noting their position and orientation.
6.Non OCSI units: Cut tie-wrap and remove pressure sensor line.
7.Remove three screws that attach the board to the control panel.
8.Remove the circuit board.
NOTE:Handle the new circuit board only by the edges to prevent
electrostatic damage to the unit.
5.7.2 Circuit Board Installation
2010-2225 Rev - BPage 21 of 59
Page 22
1.Locate the circuit board to line up the attachment points.
2.Install the three mounting screws.
3.Reinstall the tubing to each end of the black sensor tube as it was before.
4.Non OCSI unit: Reinstall the pressure sensor line and tie-wrap.
5.Plug in the 7-pin connector.
6.Reinstall the control panel and the front and cabinet backs.
5.8Product Regulator Check and Setting
The product regulator enables you to set the maximum flow of oxygen output by the
Mark5 Nuvo® unit. To check for proper adjustment of the product regulator, take the
following steps:
1.Set the I/0 (ON/OFF) switch to the I (ON) position.
2.Allow the unit to run for a few minutes.
3.Connect a pressure gauge directly to the patient outlet.
5.Adjust the regulator if necessary.Turn the knob clockwise to increase the
output pressure. (Requires a 5/32 hex wrench)
6.Reinstall the cabinet front and cabinet backs.
5.8.1 Product Regulator Cleaning or Rebuilding
Clean or rebuild the product regulator if the flow meter ball fluctuates more than 1/4
of a liter or if the regulator cannot be adjusted.
I.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord,
2.Remove the front and rear cabinets.
3.Use large pliers to unscrew the mounting nut of the product regulator.
Remove from the main structure.
4.Adjust the product regulator fully counterclockwise to unload the spring. This
makes disassembly and reassembly easier.
5.Remove the diaphragm. (Clean or replace it.)
6.Use a hex-head screwdriver to unscrew the diaphragm stem guide located in
the center of the regulator body to gain access to the seat,
7.Remove the seat. Be careful not to lose the spring located behind the seat.
8.Replace the seat or clean by blowing clean air on and around it.
9.With the spring behind the seat, screw the diaphragm stem guide back into
the body of the regulator. (Do not over tighten.)
10.Install a clean or replacement diaphragm.
11.Put the large spring and slip ring into the bonnet, and screw the bonnet onto
the regulator body.
12.Reinstall the regulator, mounting it securely to the main structure.
13.Reset the product regulator as described in Section 5.8.1.
5.9High or Low Pressure Switch Replacement (Standard Unit, Non OCSI
only)
Page 22 of 592010-2225 Rev - B
Page 23
The high and low pressure alarms are activated by a pressure transducer located
on the circuit board adjacent to the mains switch.
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the back and front cabinets and the control panel.
3.Disconnect the 7 pin connector from the circuit board.
4.Disconnect tubing from pressure sensor by cutting tie-wrap.
5.Remove the circuit board and replace with a new one.
6.Test the alarm system, as described in Section 2.3.
7.Reinstall the control panel and the front and back cabinets.
5.10Circuit Breaker Replacement
5-10.1Circuit Breaker Removal
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the cabinet front.
3.Disconnect the circuit breaker leads.
4.Unscrew the circuit breaker while you apply pressure to the circuit breaker
retaining ring.
5.10.2 Circuit Breaker Installation
Follow the removal procedure for the circuit breaker in reverse order to install the
new circuit breaker.
5.11I/0 (ON/OFF) Power Switch Replacement
5.11.1 I/0 (ON/OFF) Power Switch Removal
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position and unplug the power
cord.
2.Remove both the front and back covers.
3.Unscrew the eight Phillips-head screws that hold the control panel to the
main structure.
4.Disconnect the I/0 (ON/OFF) switch leads from the back of the switch being
careful to note the position of each.
5.Push on the back of the power switch, while holding in its four retaining tabs,
and remove the switch through the front of the control panel.
5.11.2 I/0 (ON/OFF) Power Switch Installation
Follow the removal procedure for the I/0 (ON/OFF) power switch in reverse order to
install a new power switch.
2010-2225 Rev - BPage 23 of 59
Page 24
5.12Buzzer Replacement
The buzzer is a fixed component on the circuit board and is not individually
replaceable.
5.13Hour Meter Replacement
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the cabinet back.
3.Disconnect the hour meter leads.
4.Push hour meter mounting tabs inward from the hour meter.
5.Remove the hour meter from the main structure.
6.Install the new hour meter into its mounting location, and push the mounting
tabs outward to secure hour meter. Make sure that the hour meter is
mounted right side up.
7.Reconnect the hour meter leads.
8.Reinstall the cabinet back.
5.14Flow Meter Replacement
5.14.1 Flow Meter Removal
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the cabinet back and front and then the control panel. Ref. 5.2.3.
On units with OCSI, it is necessary to also first remove the circuit board.
3.Remove the 3/8-inch silicone oxygen tubing from the flow meter fittings.
4.Unscrew the flow meter nuts with a wrench.
5.Remove the flow meter through the control panel.
5.14.2 Flow Meter Installation
To install a new flow meter, follow the flow meter removal procedure in reverse
order. Then perform a leak test on the connections.
5.15Power Cord Replacement
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position and unplug the power
cord.
2.Remove the cabinet back and front.
3.Slide the power cord strain relief reinforcement upwards to remove it from the
mounting location at the rear of the base.
4.Disconnect the power cord leads from the terminal quick connects.
5.Connect the leads on the new power cord at the terminal quick connects.
6.Reinstall the power cord strain relief into the base of the unit.
7.Reconnect the front and cabinet backs.
Page 24 of 592010-2225 Rev - B
Page 25
6.0Troubleshooting
6.1Air Pressure Test (P1)
Testing the operating pressure is a useful diagnostic tool when a concentrator has
low purity and requires servicing. Units functioning normally do not require operating
tests.
Use the following procedure to test the operating pressure of the unit.
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the cabinet rear.
3.Remove the test port plug at the top of the air tank.
4.Connect the pressure test gauge to the test port.
5.Plug in the power cord, and set the I/0 (ON/OFF) power switch to the ON
position. Set the flow meter to 5 l/min, and allow the unit to run at least five
minutes.
6.Observe the maximum and minimum readings on the pressure test gauge.
7.The maximum reading should not exceed 34 psig (235 kPa). The minimum
reading should not be less than 16 psig (110 kPa).
NOTE: When you turn the unit on, it will take several minutes to reach
normal operating pressures.
6.1.1 High Operating Air Pressure
Higher than normal operating pressure may indicate any of the following:
► A restrictive exhaust muffler, which does not allow the waste (purge) gas
to exit the system freely.
Operate the unit with the exhaust muffler disconnected to see if the
operating pressure returns to normal.
► An improperly operating control valve, confirm that the control valve is
turning at 4 rpm. Time the exhaust pulse at 7.5 seconds.
► Contaminated sieve beds. Change the sieve beds.
6.1.2 Low Operating Air Pressure
2010-2225 Rev - BPage 25 of 59
Page 26
Lower than normal operating pressure may indicate any of the following:
► A restriction in the suction resonator or inlet air filter, which limits the
amount of room air available to the compressor. Disconnect the suction
tube at the compressor, and allow the unit to operate without the suction
resonator to see if normal operating pressure returns.
► An improperly operating control valve. Confirm that the control valve does
not have a leak.
► A leak in the unit, which allows system pressure to escape. Leak test the
unit.
► A compressor with reduced output.
Ensure that the concentration level at the desired liter flow is within specifications
listed in section 2.4. If it is below specifications, replace or repair the compressor.
6.2 Product Pressure Test (P2)
Testing the product pressure is a useful diagnostic tool when a concentrator has low
purity and requires servicing. Units functioning normally do not require operating
tests.
Use the following procedure to test the product pressure of the unit.
1.Set the I/0 (ON/OFF) switch to the 0 (OFF) position, and unplug the power
cord.
2.Remove the cabinet rear.
3.Remove the test port plug from the tee at the top of the sieve bed.
4.Note:The standard unit without OCSI does not have a test port; use the
pressure sensor tube as the test connection.
5.Connect the pressure test gauge to the P2 test port.
6.Plug in the power cord, and set the I/0 (ON/OFF) power switch to the ON
position. Set the flow meter to 5 l/min, and allow the unit to run at least five
minutes.
7.Observe the maximum and minimum readings on the pressure test gauge.
The maximum reading should not exceed 16 psig (110 kPa). The minimum
reading should not be less than 9 psig (62 kPa).
6.2.1 Low Product Pressure
Lower than normal operating pressure may indicate any of the following:
► An inlet air filter that limits the amount of room air available to the
compressor. Disconnect the suction tube at the compressor, and allow
the unit to operate without the suction resonator to see if normal operating
Page 26 of 592010-2225 Rev - B
Page 27
pressure returns.
► An improperly operating control valve. Confirm that the control valve does
not have a leak.
► A leak in the unit, which allows system pressure to escape. Leak test the
unit.
► A compressor with reduced output. Ensure that the concentration level at
the desired liter flow is within specifications listed in Section 2.4. If it is
below specification, replace or repair the compressor.
6.2.2 High Product Pressure
Higher than normal operating pressure may indicate any of the following:
► A restrictive exhaust muffler, which does not allow the waste (purge) gas
to exit the system freely.
► Operate the unit with the exhaust muffler disconnected to see if the
operating pressure returns to normal.
► Check exhaust muffler and hoses for any restrictions.
► An improperly operating control valve, confirm that the control valve is
turning at 4 rpm. Time the exhaust pulse at 7.5 seconds.
► Contaminated sieve beds. Change the sieve beds.
6.3General Troubleshooting
Before reviewing the troubleshooting chart, the following steps may be useful to
isolate any malfunctions:
1.Turn the concentrator on. If unit does not turn on, refer to troubleshooting
chart.
2.Make sure all filters are clean.
3.Turn flow meter completely open, up to the highest setting. The ball should
rest at the top of the scale. If setting is not greater than 5.5 l/min, adjust
regulator so that the ball level exceeds 5.5 l/min with the flow meter
completely open.
4.Connect test pressure gauge to the outlet fitting of the unit.The pressure
should read approximately 7 psig (50 kPa).
5.Connect test pressure gauge to the P1 test port on the air tank.The
pressure should be cycling between approximately 16 and 34 psig (110 and
235 kPa).
6.Make sure the unit is cycling properly by observing the pressure gauge cycle
2010-2225 Rev - BPage 27 of 59
Page 28
between a high and a low pressure. If the unit is not cycling properly, refer to
troubleshooting chart.
7.Make sure that the unit is leak free by testing all tubing connections and
fittings with leak testing solution. Protect circuit board from solution and start
leak test at the heat exchanger, following the air flow through the unit to the
oxygen outlet. Repair all leaks by tightening connections and fittings.
8.Set the concentrator at 5 l/min and connect pressure test gauge to P2 at the
top of the sieve beds.Determine pressure parameters by observing high
andlowpressurepointsonthegauge.Itshouldcyclebetween
approximately 9 psig and 16 psig (62 to 110 kPa). If pressures are high or
low, refer to the troubleshooting chart.
9.Review troubleshooting chart to isolate and repair any other malfunctions.
The following diagnostic flow chart will help to isolate potential problems.
Page 28 of 592010-2225 Rev - B
Page 29
LowOxygen
Concentration
Verify Oxygen
Flow Rate
Measure Air
Pressure
Low PressureHigh Pressure
Replace Air
Inlet Filter
Check for
Leaks
Check the
Compressor
Normal Air
Pressure
Measure the
Oxygen Pressure
Low PressureHigh Pressure
Check for
Leaks
Replace
Wick
Replace
Muffler
Foams
Check
Control
Valve
Replace
Muffler
Foams
Check the
Control
Valve
Normal Pressure
Check for leaks at the:
- regulator outlet
- product tubing
- oxygen outlet
Replace
Sieve
Module
2010-2225 Rev - BPage 29 of 59
Page 30
6.4
Troubleshooting Chart
Problem
Probable
Cause
Solution
Compressor does not run.
onnections
No power to unit.
Check wall outlet for power.
Constant audible alarm with
I/0 (ON/OFF) power switch
in ON position.
Compressor runs with
intermittent alarm.
Concentration at 5 L/MIN is
within specifications.
Compressor shuts down
intermittently,
Defective high or low
pressure switch.
Kinked tubing.
Restricted air flow through
unit.
Unit overheating due to
improper location.
Reset or replace circuit
breaker.
Check electrical
connections.
Check power switch.
Replace I/0 (ON/OFF)
power switch.
Replace and retest pressure
switch.
Check tubing that joins the
tops of the sieve beds.
Clean inlet air filter, or
remove obstruction.
Locate unit away from
heating source, providing
adequate ventilation on all
sides.
Defective cabinet fan.
Compressor does not start.
I/0 (ON/OFF) power switch
in ON position, intermittent
alarm, and cabinet fan turns.
Compressor runs with
intermittent low pressure
alarm and low oxygen
concentration.
Page 30 of 592010-2225 Rev - B
Extreme cold start.
Compressor thermally cut
off due to excessive heat.
NOTE: It will not restart unit
it cools down,
Defective capacitor.
Faulty electrical connection
for compressor.
LeakLeak test and repair leak.
Replace cabinet fan.
Allow unit to reach room
temperature.
Blocked air intake or
defective cabinet fan/clear
obstruction, or replace
cabinet fan.
Replace capacitor.
Check electrical c
for compressor.
Page 31
Problem
Probable Cause
Solution
Compressor runs with
intermittent high pressure
alarm and low oxygen
concentration.
The tools needed for you to properly service the Mark5 Nuvo® unit are listed below:
► Requires no special tools; generally available tools including common pliers, channel lock,
wire cutters, needle-nose pliers, slotted-head screwdriver, long Phillips head screwdriver, 8inch adjustable wrench, 7/16-inch socket, 7/16-inch combination wrench, 5/8-inch
combination wrench and 3/8-inch combination wrench.
► For convenience, it is desirable to have a battery operated drill motor available to remove
and install screws.
► An accurate pressure test gauge to take both high and low pressure readings on the Mark5
Nuvo® unit should be kept available at all times. This gauge connects to the pressure test
ports on top of the air tank and on top of the sieve bed.
Appendices
Exploded Drawings
Base AssemblyA-1, A-1.1
Main Structure AssemblyA-2, A-3
Pressure Regulator AssemblyA-4
Compressor AssemblyA-5, A-5.1
Control Panel AssemblyA-6, A-6.1, A-7, A-7.1, A-8, A-9
Air Tank AssemblyA-10, A-10.1
Front Cabinet AssemblyA-11, A-11.1
Rear Cabinet AssemblyA-12, A-12.1
Sieve ModuleA-13
Refer to Thomas Compressor Manual (FSM 0159 Rev A dtd 07/04 for compressor rebuild
procedures. Call Nidek Medical customer service to obtain a pdf file copy.
2010-2225 Rev - BPage 33 of 59
Page 34
A-1 BASE ASSEMBLY
NUVO 0100-0300 REV A
NOTE: USE THIS DRAWING ON UNITS EARLIER THAN SERIAL # 062-11663
Page 34 of 592010-2225 Rev - B
Page 35
A-1.1 BASE ASSEMBLY
Nuvo 0100-0300Q Rev B
NOTE: USE THIS DRAWING ON UNITS AFTER SERIAL # 062-11663
2010-2225 Rev - BPage 35 of 59
Page 36
A-2 MAIN STRUCTURE ASSEMBLY
FRONT VIEW
NUVO 0140-0300 REV C
Page 36 of 592010-2225 Rev - B
Page 37
A-3 MAIN STRUCTURE ASSEMBLY
REAR VIEW
NUVO 0140-0300 REV C
2010-2225 Rev - BPage 37 of 59
Page 38
A-4 REGULATOR ASSEMBLY
NUVO 0160-0300 REV A
Page 38 of 592010-2225 Rev - B
Page 39
A-5 COMPRESSOR ASSEMBLY
NOTE: USE THIS DRAWING ON UNITS EARLIER THAN SERIAL # 062-11663
Nuvo 0200-0300 Rev. A
2010-2225 Rev - BPage 39 of 59
Page 40
A-5.1 COMPRESSOR ASSEMBLY
NOTE: USE THIS DRAWING ON UNITS AFTER SERIAL # 062-11663
Nuvo 0200-0350 Rev. B
Page 40 of 592010-2225 Rev - B
Page 41
A-6 CONTROL PANEL ASSEMBLY
UNIT WITH OCSI
FRONT VIEW
NOTE: USE THIS DRAWING ON UNITS EARLIER THAN SERIAL # 062-11663
Nuvo 0300-0330 Rev. A
2010-2225 Rev - BPage 41 of 59
Page 42
A-6.1 CONTROL PANEL ASSEMBLY
UNIT WITHOUT OCSI
FRONT VIEW
NOTE: USE THIS DRAWING ON UNITS AFTER SERIAL # 062-11663
Nuvo 0300-0300 Rev. B
Page 42 of 592010-2225 Rev - B
Page 43
A-7 CONTROL PANEL ASSEMBLY
UNIT WITH OCSI
REAR VIEW
NOTE: USE THIS DRAWING ON UNITS EARLIER THAN SERIAL # 062-11663
Nuvo 0300-0330 Rev. A
2010-2225 Rev - BPage 43 of 59
Page 44
A-7.1 CONTROL PANEL ASSEMBLY
UNIT WITH OCSI
REAR VIEW
NOTE: USE THIS DRAWING ON UNITS AFTER SERIAL # 062-11663
NUVO 0300-0330 REV.B
Page 44 of 592010-2225 Rev - B
Page 45
A-8 CONTROL PANEL ASSEMBLY
STANDARD UNIT WITHOUT OCSI
FRONT VIEW
NUVO 0300-0300 Rev A
2010-2225 Rev - BPage 45 of 59
Page 46
A-9 CONTROL PANEL ASSEMBLY
STANDARD UNIT WITHOUT OCSI
REAR VIEW
NUVO 0300-0300 Rev A
Page 46 of 592010-2225 Rev - B
Page 47
A-10 AIR TANK ASSEMBLY
NOTE: USE THIS DRAWING ON UNITS EARLIER THAN SERIAL # 062-11663
NUVO 0350-0300 REV. B
2010-2225 Rev - BPage 47 of 59
Page 48
A-10.1 AIR TANK ASSEMBLY
NOTE: USE THIS DRAWING ON UNITS AFTER SERIAL # 062-11663
NUVO 0350-0300 REV. B
Page 48 of 592010-2225 Rev - B
Page 49
A-11 FRONT CABINET ASSEMBLY
Nuvo 0500-0300 Rev. A
2010-2225 Rev - BPage 49 of 59
Page 50
A-11.1 FRONT CABINET ASSEMBLY
Nuvo 0500-0300 Rev. B
Page 50 of 592010-2225 Rev - B
Page 51
A-12 REAR CABINET ASSEMBLY
NUVO 0550-0300 REV A
2010-2225 Rev - BPage 51 of 59
Page 52
A-12.1 REAR CABINET ASSEMBLY
Nuvo 0550-0300 Rev. B
Page 52 of 592010-2225 Rev - B
Page 53
A-13 SIEVE MODULE ASSEMBLY
NUVO 0600-0300 Rev A
2010-2225 Rev - BPage 53 of 59
Page 54
REPLACEMENT PARTS LISTING
BASE ASSEMBLY
MAIN STRUCTURE ASSEMBLY
REGULATOR ASSEMBLY
Item numbers reference call-out bubbles on the illustrations
99250-1050SCREW, 10-32 X 3/8 PAN HD.PHIL8EA
109250-1040O-RING, 5.0" ID X .125THICK2EA
119250-1048WASHER,NYLON .44"IDX.75"X.062"1EA
129007-6G32HUMIDIFIER FITTING DISS1EA
139250-1039COVER,PRESS TO RESET 3/8"1EA
159250-1009FLOWMETER, 0-5 LPM1EA
169250-1011BREAKER,CIRCUIT 10 AMP1EA
16a9250-1010BREAKER, CIRCUIT 5 AMP1EA
2010-2225 Rev - BPage 55 of 59
Page 56
189250-1038NUT,HEX ,NICKEL 3/8"-271EA
CONTROL PANEL ASSEMBLY (STD
–
NON OCSI)
AIR TANK ASSY,NUVO
199250-1021HUMIDIFIER BLOCK1EA
207854-6052HOSE 5/32 X 11/32 X 2 LG SILIC1EA
217854-6054HOSE 5/32 X 11/32 X 10"LG SIL1EA
227854-6055HOSE 5/32 X 11/32 X 7"LG SIL1EA
19250-1005PANEL,CONTROL1EA
29250-1090BOARD, STD NON-OCSI1EA
39250-1045SCREW,PLASTITE#4X3/8" PAN.HD2EA
47854-6048HOSE 1/16 X 3/16 X 5 LONG SILI1EA
56491-1007ADAPTER 5/32 X 3/32 HOSE BARB1EA
67854-6050HOSE 5/32 X 11/32 X 6 LONG SIL1EA
76491-1006ADAPTER 1/4 ODT X 3/16 HOSE1EA
89250-1041HOSE 5/32 X 11/32 X 5 LONG SIL1EA
97631-1053FILTER, BACTERIAL MK-51EA
107854-6052HOSE 5/32 X 11/32 X 2 LG SILIC1EA
116956-9674VALVE CHECK 1/4 HOSE MPC A 9751EA
129250-1012SWITCH,POWER 110 VOLT1EA
12a9250-1013SWITCH,POWER 230 VOLT1EA
139250-1050SCREW, 10-32 X 3/8 PAN HD.PHIL8EA
149250-1040O-RING, 5.0" ID X .125THICK2EA
159250-1048WASHER,NYLON .44"IDX.75"X.062"1EA
169007-6G32HUMIDIFIER FITTING DISS1EA
179250-1039COVER,PRESS TO RESET 3/8"1EA
199250-1009FLOWMETER, 0-5 LPM1EA
209250-1011BREAKER,CIRCUIT 10 AMP1EA
20a9250-1010BREAKER, CIRCUIT 5 AMP1EA
229250-1038NUT,HEX ,NICKEL 3/8"-271EA
239250-1021HUMIDIFIER BLOCK1EA
247854-6054HOSE 5/32 X 11/32 X 10"LG SIL1EA
257854-6055HOSE 5/32 X 11/32 X 7"LG SIL1EA
999030-6008TIE, WRAP 4~1EA
19250-1031TUBE,AIR TANK ALUM 3/8"1EA
29250-1019BRACKET,AIR TANK1EA
36134-0916SCREW,10-32 X 1/2~ RD PHILLIPS1EA
49250-1037NUT,10-32 ,LOCKNYLON INSERT1EA
59250-1056FITTING,BRASS AIR TANK1EA
67355-4775CONNECTOR, STRAIGHT 1/8~MNPT X2EA
79250-1055TANK, AIR 6"O.D. X 10" LG1EA
89007-4G25WICK ASSY.1EA
99250-1026CLAMP, HOSE NYLON.67"-.78"ID2EA
Page 56 of 592010-2225 Rev - B
Page 57
109250-1053HOSE 1/2"ID X 3/4"OD X 10.125"1EA
POWER CORD ASSEMBLY
CABINET FRONTASSEMBLY
CABINET BACK ASSEMBLY
MODULE ASSEMBLY
LABELS
SHIPPING MATERIAL
119200-1006FITTING, QUICK DISCONNECT1EA
129200-1612HOSE, 1/4 OD X 18 LG1EA
19250-1311CORD,POWER CONC (US)1EA
1A9250-1330
19250-1002CABINET,FRONT NUVO1EA
29250-1050SCREW, 10-32 X 3/8 PAN HD.PHIL4EA
19250-1001CABINET,BACK NUVO1EA
29250-1006DOOR,ACCESS NUVO1EA
39250-1025FILTER,CABINET INLET1EA
49250-1050SCREW, 10-32 X 3/8 PAN HD.PHIL4EA
CORD,POWER CONC (Europe)
19250-8005
29022-8G06
1A9250-8008
2A9022-8G07MODULE 230 V 50 HZ , REBUILT1EA
19250-1076LABEL,FRONT STD.1EA
1A9250-1078LABEL, FRONT W/OCSI1EA
29250-1070LABEL FRONT "NUVO"1EA
39250-1071LABEL,TOP WARNING ICON1EA
49250-1075LABEL BACK 115/601EA
4A9250-1077LABEL BACK CE1EA
72010-2224FOPERATING GUIDE, STD NUVO1EA
7A2010-2224CEOPERATING GUIDE, CE MODEL1EA
19250-1600CARTON, CONCENTRATOR NUVO1EA
29250-1601PACK, BOX TOP1EA
39250-1602PACK, BOX BOTTOM1EA
MODULE 115 V 60 HZ NEW
MODULE 125 V 60 HZ REBUILT
MODULE 230 V 50 HZ NEW
1EA
1EA
1EA
19012-8780CANNULA W/7 FT TUBING1EA
29012-8781TUBING EXTENSION 25 FT1EA
39012-8774HUMIDIFIER 350 CC1EA
49012-8783HOSE CONNECTOR1EA
59012-8785ADAPTER DISS TO HOSE1EA
2010-2225 Rev - BPage 57 of 59
ACCESSORIES
Page 58
Nidek Medical Oxygen Concentrator Service and Maintenance Log
Model Number ________________
Initial Inspection
1. Upon receipt, check the unit for shipping
damage. Notify shipping company if damaged.
2. Verify that cabinet air filter and the inlet air filter
are in place.
3. Plug the unit into an electrical outlet, turn the unit
'ON,’ and check the audible/visual alarms.
4. Set the flow meter/flow control at the maximum
recommended flow rate and allow the unit to run for
15 minutes.
5. Using a calibrated oxygen analyzer, verify
concentration is greater than 87 percent.
Routine Service Check
Perform routine servicing as shown in the chart
below. Record the activities performed in the log
provided on the following page.
1. Record the elapsed usage time in hours.
2. Check oxygen concentration with a calibrated
oxygen analyzer.
3. Verify audible alarm and indicator light functions
between patients and every two years.
4. Inspect filters and replace as necessary.
Serial Number ___________________
Between-Patient Maintenance
1. Remove oxygen tubing, cannula, and humidifier
bottle and discard.
2. Wash or replace the humidifier tubing if used.
3. Wash or replace the cabinet air filter.
4. Clean the concentrator cabinet.
5. Check oxygen concentration and flow. If the unit
performs within specification, the final product
filter does not need to be replaced between patients.
Patient/Caregiver Maintenance
1. Inspect the Oxygen tubing, cannula, and
humidifier bottle - clean as needed according to
manufacturer’s instructions.
2. Wash the cabinet air filter weekly with a mild
detergent solution. Dry before reinstalling onto the
device.
The routine service intervals shown below depend
on the conditions in which the devices are used.
They reflect the minimum recommendation when
operated in a clean environment. As conditions can
vary widely, the homecare provider or patient
caregiver is responsible to determine:
- the character of the environment in which the
concentrator is to operate.
- a maintenance schedule with intervals based on
the environment in which the unit is
operating/functioning.
Standard Servicing Intervals are shown below. Intervals used by the homecare service provider
and/or patient caregiver should be more frequent when conditions of usage dictate.
Nidek Medical Oxygen Concentrator Routine Service Intervals
Check Percent
Oxygen
Concentration
OCSI Models: Every
15,000 hours
or 3 years.
Std Models: Every
5,000 hours or 1
year.
Page 58 of 592010-2225 Rev - B
Cabinet Air FilterInlet Air FilterFinal Product FilterCapacitor
Wash the filter
each week in a
mild detergent
solution.
Dry before
reinstalling.
Inspect at each
patient visit. Replace
annually, or more
often depending on
environment.
Replace at each
compressor
service / module
replacement.
Replace at each
compressor
service / module
replacement.
Page 59
Please maintain a log of all maintenance
activities performed on this unit.
Serial Number__________Model_____________
DateHours% O2
Inspection Prior to Putting Into Service
In-Service Checks
Alarms
Check
Additional Information (Work Done, Filter Changes,
Comments, etc)
Medical device regulations require users and service personnel to notify manufacturers of any
incidents that, if repeated, could cause injury to any person.
email: info@nidekmedical.com
Please update maintenance log information upon each service at www.nidekmedical.com under
the 'Maintenance Log' tab.
2010-2225 Rev - BPage 59 of 59
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