Nidek Medical Mark 5 Nuvo Lite Series Instructions For Use Manual Download Page 2

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2010-8401CE-E 

February 2018 

Page 2 of 8 

GLOSSARY OF SYMBOLS 

ON (Power switched on) 

OFF (Power switched off) 

Manufacturer Name and Address 

Type B Device 

Class II Protection 

IPX1 

Protection from vertically falling water drops 

Do Not Expose to Open Flames 

Do Not Expose to Oil or Grease 

Tools Required / Technician Only 

Refer to Technical Information / Service Manual 

Refer to Instructions for Use / User’s Guide 

Keep in Vertical Position 

FRAGILE – Handle with Care 

Visual Alarm Indicator 

WARNING – A hazard or unsafe practice that 

can result in serious injury or death if 
conditions are not avoided. 
Caution - A hazard or unsafe practice that can 

result in minor injury and / or property damage 
if conditions are not avoided. 

Note – Information important enough to 
emphasize or repeat 

YOUR DEVICE 

2.1 

Intended Use and Operation 

The Mark 5 Nuvo Lite Family (Nuvo Lite and Nuvo Lite 
3)  Oxygen  Concentrators  are  used  as  a  means  of 
providing  continuous  oxygen  enriched  product  gas  for 
patients,  adolescent  to  geriatric,  suffering  from  health 
conditions  that  cause  low  levels  of  oxygen  in  the  blood 
(hypoxaemia). 

To  ensure  your  safety,  use only  after  one  or  more 

settings have been individually determined or prescribed 

for you at your specific activity levels – AND – only use 
the accessories that were used when your settings were 

determined. 
While undergoing oxygen therapy, if you feel discomfort 

or  experience  a  medical  emergency,  seek  medical 
assistance immediately. 

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 
resonator  and  fine  filter.    Pressurized  air  then  exits  the 
compressor  and  passes  through  a  heat  exchanger,  which 
reduces the temperature of the compressed air.  Next, an 
electronic  valve  system  directs  the  air  into  one  of  two 
tubes  that  contain  molecular  sieve  (sieve  beds).    The 
molecular sieve adsorbs (physically attracts) the nitrogen 
from the air as it is pushed through the sieve beds.  This 
allows  the  oxygen  enriched  product  gas  to  pass  through 
before being delivered to the pressure regulator.  As one 
tube  is  generating  the  product  gas,  the  other  is  being 
purged  of  the  adsorbed  nitrogen,  this  process  is  called 
pressure swing adsorption (PSA).  After passing through 
the  regulator,  the  rate  of  product  gas  being  delivered  to 
the  patient  is  set  by  the  flow  meter  adjusting  valve.  
Finally,  it  passes  through  a  fine  particle  filter  and  then 
over a sensor that detects the oxygen concentration of the 
product  gas  before  it  exits  the  device  through  a  fire 
resistant outlet. 

2.2 

Device Features 

Front panel (Fig. 1) 

1 – Flow adjustment knob 

4 – Circuit Breaker 

2 – Oxygen Product Outlet 

5 – Indicator Lights

3 – Mains Power Switch 

  (green and yellow)

Rear panel (Fig. 2) 

6 – Humidfier (space reserved)

9 – Air Filter / Grill 

7 – Technical Label

(Inlet Filter under – Fig 5)

8 – Mains Cable

10 – Hour Meter

Summary of Contents for Mark 5 Nuvo Lite Series

Page 1: ... 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...

Page 2: ...e used when your settings were determined While undergoing oxygen therapy if you feel discomfort or experience a medical emergency seek medical assistance immediately 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 resonator and fine filter Pressurized air then exits the compressor an...

Page 3: ...pplied the device has a Blockage Alarm A continuous audible alarm and both indicator lights will be lit immediately in the event the flow of oxygen to patient becomes blocked Malfunction 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 Power Switch Fig ...

Page 4: ...mance and void the manufacturer s responsibility Spare Parts Part Ref Cabinet air filter Fig 2 9 8400 1025 Inlet Filter Under Fig 2 9 8400 1180 Ventilation Grill Fig 2 9 8400 0108 Casters 8300 8068 Mains Cable Wrap 8400 0022 Please consult the Nuvo Lite Maintenance Manual PN 2010 8405 for instructions on replacing any above spare parts 3 UNPACKING AND INSPECTION The Oxygen Concentrator is packaged...

Page 5: ...s or other by placing the orifice s on the surface of a glass of water The flow should disturb the surface 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 3 to the O OFF position to stop the device The oxygen enriched air flow continues for approximately one minute after the device is stopped Make sure during operatio...

Page 6: ...vidual product markings for disposal Furthermore as part of the marking directive 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 the I ON position but the device does not operate Mains cable Fig 2 8 is not correctly plugged into the wall outlet Check...

Page 7: ...______________________________________________________________________________________________________________ 2010 8401CE E February 2018 Page 7 of 8 EN 8 EMC INFORMATION ...

Page 8: ...eriodic servicing by an approved technician do not comply with the manufacturer 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 European directive but its operation may be affected by other devices being used nearby such as diathermy and high frequency e...

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