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______________________________________________________________________________________________________________ 

2010-2324CE-G 

March  2022 

Page 1 of 8 

EN 

 
 

 
 
 

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]

 

 

 

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). 

 

 

Only 

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 
supervision of a licensed physician. 

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

 

Device Performance and 

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

 

 

NUVO 10 (Model 1005) shown for reference. 

Summary of Contents for Mark 5 Nuvo Series

Page 1: ...r 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...

Page 2: ...feel discomfort or experience a medical emergency seek medical assistance immediately The Mark 5 Nuvo Family begins their operation with air being pulled into the external air intake filter This filt...

Page 3: ...tion detection If low pressure occurs due to a mechanical failure the indicator light will flash yellow and a continuous audible alarm will actuate If any of the above alarm conditions occur press the...

Page 4: ...r spare parts which are not recommended by the manufacturer may reduce its performance and void the manufacturer s responsibility Spare Parts Part Ref Cabinet air filter Fig 2 7 9250 1025 Filter Silen...

Page 5: ...urface of the water 6 Adjust the nasal cannula to suit your face 4 3 Shut Down At the end of the treatment press the Power Switch Fig 1 1 to the O OFF position to stop the device The oxygen enriched a...

Page 6: ...e 93 42 EEC the serial number of the device disposed of must be sent to Nidek Medical if the unit has the marking 7 TROUBLESHOOTING Observations Possible Causes Solutions The I O ON OFF button is in t...

Page 7: ...____________________________________________________________________________________________________ 2010 2324CE G March 2022 Page 7 of 8 EN be powered from an uninterruptable power supply UPS 8 EMC I...

Page 8: ...r s specifications the manufacturer is not responsible in the event of an accident or non performance This device complies with the requirements of the FDA Quality System Regulation and 93 42 EEC Euro...

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