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INSTRUCTIONS FOR USE
Mark 5 Nuvo Lite Family
(Nuvo Lite and Nuvo Lite 3)
OXYGEN CONCENTRATOR
For models: 525, 535, 925 and 935
(and variants thereof)
[Original language is English]
This unit is not a life-support device. Geriatric,
pediatric, or any other patient unable to
communicate discomfort while using this device
should receive additional monitoring.
This device supplies highly concentrated oxygen
enriched product gas that promotes rapid
burning.
DO NOT allow smoking or open flames within the
same room of this device or the administration
accessory (cannula). Failure to observe this
warning can result in severe fire, property
damage, and / or cause physical injury or death.
Oxygen accelerates the combustion of flammable
substances. DO NOT use oil, grease, petroleum
based or other flammable products on the
device, the administration accessory (cannula) or
the patient's face / neck.
Only persons who have read and understood this
entire manual should be allowed to operate the
device.
CONTRAINDICATIONS - Those who continue to
smoke (because of the increased fire risk and the
probability that the poorer prognosis by smoking
will offset the treatment benefit).
Federal Law (US) restricts this device to sale by, or
℞
on the order of, a licensed physician. This oxygen
concentrator should be used only under the
Only
supervision of a licensed physician.
______________________________________________________________________________________________________________
2010-8401CE-E
Contents
1
GLOSSARY OF SYMBOLS ................... 2
2
YOUR DEVICE ....................................... 2
2.1
2.2
2.3
2.4
Specifications ............................................... 3
2.5
3
UNPACKING AND INSPECTION ......... 4
4
INSTALLATION AND OPERATION .... 4
4.1
4.2
4.3
5
CLEANING AND MAINTENANCE ...... 5
5.1
5.2
6
DISPOSAL ............................................... 6
6.1
6.2
7
TROUBLESHOOTING ........................... 6
8
EMC INFORMATION............................. 7
9
CONFORMITY WITH EN 60601-1 ........ 8
February 2018
Nuvo Lite (Model 925) shown for reference.
Intended Use and Operation .............. 2
Device Features ................................. 2
Alarms and Safety Features............... 3
Accessories and Spare Parts .............. 4
Installation ......................................... 4
Start-Up ............................................. 5
Shut Down ......................................... 5
Cleaning ............................................ 5
Maintenance ...................................... 5
Method for Waste Disposal ............... 6
Disposing of the Device .................... 6
EN
Page 1 of 8
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Related Manuals for Nidek Medical Nuvo Lite 925
Summary of Contents for Nidek Medical Nuvo Lite 925
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Page 1: Instructions For Use
INSTRUCTIONS FOR USE Mark 5 Nuvo Lite Family (Nuvo Lite and Nuvo Lite 3) OXYGEN CONCENTRATOR For models: 525, 535, 925 and 935 (and variants thereof) Nuvo Lite (Model 925) shown for reference. [Original language is English] This unit is not a life-support device. Geriatric, Contents pediatric, or any other patient unable to communicate discomfort while using this device... -
Page 2: Nuvo Lite And Nuvo Lite
GLOSSARY OF SYMBOLS The Mark 5 Nuvo Lite Family begins their operation with air being pulled into the external air intake filter. This filtered air enters the compressor via a suction ON (Power switched on) resonator and fine filter. Pressurized air then exits the OFF (Power switched off) compressor and passes through a heat exchanger, which reduces the temperature of the compressed air. -
Page 3: Alarms And Safety Features
Use the power cord provided. Electrical protection: Check that the electrical characteristics of the power • A 5A circuit breaker is incorporated into the front outlet used match those indicated on the manufacturer’s cabinet of all 230V models technical label (Fig 2-7) on the rear panel of the device. •... -
Page 4: Accessories And Spare Parts
European Directive, or any other applicable regulatory requirements. The Oxygen Concentrator is packaged to protect the The accessories below, available from Nidek Medical device from damage while being transported and stored. Products, Inc. and our distributors, comply with these After the device is removed from the package, inspect requirements. -
Page 5: Start-Up
Shut Down Device must have power to operate. In the event of power loss and for continued operation a backup source is At the end of the treatment, press the Power Switch (Fig recommended. 1-3) to the “O” (OFF) position to stop the device. The Do not use in a specifically magnetic environment (MRI, X- oxygen enriched air flow continues for approximately ray, etc.). -
Page 6: Disposal
which are designated as being the manufacturer’s DO NOT disassemble due to danger of electrical shock. responsibility or by the manufacturer as repairable. Refer servicing to qualified service personnel. DISPOSAL The expected service life of this device is 10 years with routine preventive and required maintenance. -
Page 7: Emc Information
EMC INFORMATION ______________________________________________________________________________________________________________ 2010-8401CE-E February 2018 Page 7 of 8... -
Page 8: Conformity With En 60601-1
EN 60601-1-2 standard. EU Representative mdi Europa GmbH Langenhagener Str. 71 30855 Hannover-Langenhagen Germany Nidek Medical Products, Inc. Tel: +49-511-39-08 95 30 3949 Valley East Industrial Drive Fax: +49-511-39-08 95 39 Birmingham, Alabama 35217 U.S.A. info@mdi-europa.com Tel: 205-856-7200 Fax: 205-856-0533 www.mdi-europa.com...
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