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INSTRUCTIONS FOR USE
Mark 5 Nuvo Family
(NUVO, NUVO 8 & NUVO 10)
OXYGEN CONCENTRATOR
For models: 505, 565, 585, 595, 905, 965, 985 and 1005
[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
Only
concentrator should be used only under the
supervision of a licensed physician.
______________________________________________________________________________________________________________
2010-2324CE-G
(and variants thereof)
March 2022
NUVO 10 (Model 1005) shown for reference.
Contents
1
GLOSSARY OF SYMBOLS ................... 2
2
YOUR DEVICE ....................................... 2
2.1
Intended Use and Operation .............. 2
2.2
Device Features ................................. 2
2.3
Alarms and Safety Features............... 3
2.4
Specifications ............................................... 3
2.5
Accessories and Spare Parts .............. 4
3
UNPACKING AND INSPECTION ......... 4
4
INSTALLATION AND OPERATION .... 4
4.1
Installation ......................................... 4
4.2
Start-Up ............................................. 5
4.3
Shut Down ......................................... 5
5
CLEANING AND MAINTENANCE ...... 5
5.1
Cleaning ............................................ 5
5.2
Maintenance ...................................... 5
6
DISPOSAL ............................................... 6
6.1
Method for Waste Disposal ............... 6
6.2
Disposing of the Device .................... 6
7
TROUBLESHOOTING ........................... 6
8
EMC INFORMATION............................. 7
9
CONFORMITY WITH EN 60601-1 ........ 8
EN
Page 1 of 8
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Summary of Contents for Nidek Medical Mark 5 Nuvo Series
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Page 1: Table Of Contents
INSTRUCTIONS FOR USE Mark 5 Nuvo Family (NUVO, NUVO 8 & NUVO 10) OXYGEN CONCENTRATOR For models: 505, 565, 585, 595, 905, 965, 985 and 1005 (and variants thereof) [Original language is English] NUVO 10 (Model 1005) shown for reference. This unit is not a life-support device. -
Page 2: Glossary Of Symbols
GLOSSARY OF SYMBOLS The Mark 5 Nuvo Family begins their operation with air being pulled into the external air intake filter. This filtered air enters the compressor via a suction resonator ON (Power switched on) and fine filter. Pressurized air then exits the compressor and passes through a heat exchanger, which reduces the OFF (Power switched off) temperature of the compressed air. -
Page 3: Alarms And Safety Features
Electrical protection: Use the power cord provided. 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 plate on the rear panel of the device. ... -
Page 4: Accessories And Spare Parts
European Directive, or any other applicable regulatory requirements. UNPACKING AND INSPECTION The accessories below, available from Nidek Medical Products, Inc. and our distributors, comply with these The Oxygen Concentrator is packaged to protect the requirements. Contact your equipment supplier to obtain device from damage while being transported and stored. -
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. 1-1) 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
DISPOSAL Preventive Maintenance Wash cabinet filter (see “Cleaning and replacing filters”) weekly or after Method for Waste Disposal approximately 100 hours of use and for each new patient. More frequent cleaning is recommended in dusty All waste from the device (Patient Circuit, Molecular environments. -
Page 7: Emc Information
EMC INFORMATION be powered from an uninterruptable power supply (UPS). ______________________________________________________________________________________________________________ 2010-2324CE-G March 2022 Page 7 of 8... -
Page 8: Conformity With En 60601-1
CB and other portable devices, microwave ovens, induction plates or even remote control toys or any other electromagnetic interferences which exceed the levels specified by the EN 60601-1-2 standard. Nidek Medical Products, Inc. 3949 Valley East Industrial Drive Birmingham, Alabama 35217 U.S.A.
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