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

______________________________________________________________________________________________________________ 

2010-8401CE-E 

February 2018 

Page 5 of 8 

EN 

Inlet Filter - Figure 5 

(under air filter and grill)

Device must have power to operate. In the event of power 
loss and for continued operation a backup source is 

recommended. 

Do not use in a specifically magnetic environment (MRI, X-
ray, etc.). May cause device malfunction. 

We recommend against the use of extension cords and 
adapters, as they are potential sources of sparks and fire. 

Consult your equipment provider for further information 
regarding altitudes of 2200 m to 4000m (7500 to 13000ft). 

Complies with EN 60529:2001 + A2:2014 rating of IPX1; 

enclosure protects internal electrical components against 

vertically falling water drops. 
Complies with EN 60601-1:2006 [11.6.3]; enclosure 

protects internal electrical components against spilling of a 
glass of water (i.e. contents of humidifier). 

4.2 

Start-Up 

1) Ensure that the Power Switch (Fig 1-1) is in the “

O

(OFF) position. 

If  used  with  a  humidifier  (Fig  3):

Unscrew  the  flask 

and  fill  it  with  distilled  water  up  to  the  line  (see 
manufacturer’s  instructions).  Then  screw  the  lid  on 
the humidifier flask until there are no leaks. Connect 
the  oxygen  tube  to  the  humidifier  outlet  nozzle. 
Screw  the  humidifier directly to the provided Patient 
Hose  Kit  (tubing  and  elbow)  attached  to  the  Oxygen 
Product Outlet (Fig 1-2). Ensure that all of the parts 
are connected correctly so as to avoid leaks. 

Replace  water  in  humidifier  bottle  before  each 
treatment.

If  not  using  a  humidifier: 

Remove  the  Patient  Hose 

Kit  attached  to  the  Oxygen  Product  Outlet  (Fig  1-3) 
and connect the oxygen tube directly to the outlet. 

2)

Plug  the  power  cable  into  a  power  outlet  of  the 
correct  voltage  and  frequency  as  defined  on  the 
manufacturer’s technical label (Fig 2-7).

3)

Press  the  Power  Switch  (Fig  1-3)  to  the  ON 

I

” 

position. 

See  the  Alarms  and  Safety  Features  on  page  3  for 

indicator lights and meanings.

4) Turn  the  flow  adjustment  knob  (Fig  1-1)  to  the 

prescribed value. 

The  required  oxygen  concentration  is  normally 

obtained  within  two  minutes  after  the  device  is 
started. 

5) Check that the oxygen flows out of the administration 

device  (nasal  cannulas  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  operation  and  after  shut  down  that 

the  cannula  is  facing  away  from  soft  surfaces  and 
clothing.    Excess  oxygen  can  accumulate  and  cause 

ignition if exposed to a spark or open flame.  

After  turning  the  unit  off,  the  user  must  wait  3-5 
minutes before turning it back on. System pressure must 

dissipate before the unit will properly restart. 

CLEANING AND MAINTENANCE  

5.1 

Cleaning 

Cleaning and disinfecting your device:

 Only the outside 

of  the 

device 

is  to  be  cleaned.    After  making  sure  the 

Power Switch (Fig 1-3) is in the "

O

"

 (OFF) position, use 

a soft, dry cloth or, if necessary, a damp sponge, to wipe 
the  cabinet  enclosure.    Then  thoroughly  dry  with  wipes 
and  an  alcohol  based  solution.  To  prevent  the  spread  of 
bacteria  and  viruses,  this  should  be  done  daily  and  for 
each new patient. 

Acetone, solvents or any other flammable products must 
not be used. Do not use abrasive powders. 

Cleaning  and  replacing  filters:

  The  removable  cabinet 

air  filter  (Fig  2-9)  must  be  cleaned  in  warm  water  and 
household  detergent.    Dry 
before  reinstalling.    The  inlet  / 
silencer  filter  (see  Fig  5) 
should  be  inspected  at  each 
patient  visit  and  replaced  if 
required.  The  final  product 
filter (not pictured) should only 
be  replaced  by  a  technician  if 
required (not common). 

Cleaning  and  replacing  accessories:

  Clean  the 

humidifier  according  to  manufacturer’s  instructions.    If 
no instructions are provided, do the following: empty the 
water  from  the  humidifier,  rinse  the  flask  and  lid  under 
running  water.    Regularly  disinfect  the  humidifier  by 
immersing the flask and lid in a disinfectant solution (we 
recommend using a solution of 1 part vinegar to 10 parts 
water).  Rinse under running water and dry.  Tubing and 
cannula  should  be  used  according  to  the  manufacturer’s 
instructions and replaced for each new patient to prevent 
the spreading of bacteria and viruses. 

5.2 

Maintenance 

No  special  maintenance  needs  to  be  carried  out  by  the 
patient.  Your  equipment  supplier  performs  periodic 
maintenance  operations  to  assure  continued  reliable 
service from the 

device

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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