Nidek Medical Mark 5 Nuvo OCSI Lite 3 User Manual Download Page 9

September 2013

2010-8403CE Rev C

9

Mark 5 Nuvo Lite

Serial No. _______

_________________________________

Date fi rst used : 

__________________

Maintained by: __________________
________________________________

Your distributor: ________________

Address : _______________________
________________________________

Telephone : _____________________

PREVENTIVE MAINTENANCE

a. Wash cabinet fi lter weekly.

b. Inspect inlet air fi lter at each patient visit. 

    Replace fi lter every 2 years, or more often 

depending on environment.

c. Check oxygen concentration every 15,000

hours or 3 years of operation to verify the
continuing OCSI function.

The manufacturer’s instructions for the

preventive maintenance

of the devices are

defi ned in the maintenance manual. Check 

with your service provider for any updates to
recommended schedules. The work must be
carried out by suitably trained technicians.

Use original spare parts only (see Pg. 10)

Upon request, the supplier can provide circuit
diagrams, spare parts lists, technical details

or  any  other information  of use  to  qualifi ed 

technical personnel for parts of the device which
are designated as being the manufacturer’s
responsibility or by the manufacturer as
repairable.

Electrical power supply:

Rating:

230V 50Hz

Average Power:

180 W(avg)

Protection Class:

Class II

Mains Protection:

5A

Filters:

At the rear of the device: a cabinet air fi lter.

At the compressor input: an inlet air fi lter, 5 µm,  

located behind the cabinet air fi lter.   

Before the oxygen outlet: a fi nal product fi lter, 

< 0.3 µm. (technician only).

Air circulation

A tubeaxial fan cools the compressor compart-
ment.

Environmental limit conditions

The performances of the device (especially the
oxygen concentration) are quoted at 21

o

C (70

o

F)

and one atmosphere. They may change with
temperature and altitude. For further informa-
tion, please consult the maintenance manual Ref
# 2010-8405.

• The device must be stored, transported and

used in the vertical position only.

• Ambient temperature of between 5

o

C and

40

o

C (40

o

F to 104

o

F) operation.

• Storage temperature from -20

o

C to 60

o

C

(-4

o

F to 140

o

F).

• Relative humidity of between 15% and 95%

operation and storage, both non-condensing.

• Altitude(21

o

C): Up to 2,286m (7,500ft)

without degradation; Consult your equip-
ment provider for further information re-
garding 2,286m to 4000m (7500 to 13000
ft)

• Complies with EN60601-1 standard; spil-

ling a glass of water.

5.7. Standards

ISO 8359:1996 Oxygen concentrators for medi-
cal use.
EN 60601-1[UL60601-1:2003],CAN/CSA-
C22.2 No.601.1-M90 w/A1&A2: Electrical
Safety- Medical Devices.
EN60601-1-2:2001 Electromagnetic Compat-
ibility

Summary of Contents for Mark 5 Nuvo OCSI Lite 3

Page 1: ...gen concentration warning light GLOSSARY OF SYMBOLS Original language is English GLOSSARY OF SYMBOLS 1 GENERAL SAFETY GUIDELINES 2 1 Unpacking and Packaging 3 1 1 Method for disposing of waste 3 1 2 M...

Page 2: ...ing to quali ed service personnel GENERAL SAFETY GUIDELINES Only persons who have read and understood this entire manual should be allowed to operate the MARK 5 Nuvo Lite TheCAUTIONSbelowindicateapote...

Page 3: ...detected please contact your equipment provider Operating environmental condi tion guidelines are discussed later in another section of this User s Guide 1 1 METHOD FOR WASTE DISPOSAL All waste from t...

Page 4: ...r the humidi er bottle manufacturer s recommendation Re attach the lid to the bottle and connect to the oxygen concentrator Place the bottle on the concentrator and secure with the attachment straps a...

Page 5: ...Adjust the nasal cannula to suit your face see Fig 3 4 1 Filter Silencer 2 Cabinet lter 3 Ventilation grill Note Shown with grate removed 115V Fig 3 3 230V Fig 4 1 3 2 Turning off device Attheendofth...

Page 6: ...cuit oxygentherapynasalcannula etc must be changed 4 3 Maintenance No special maintenance needs to be carried out by the patient Your equipment supplier performs periodic maintenance operations to ass...

Page 7: ...rms No voltage detection In the event of a loss of mains power an inter mittent audible alarm is activated and the green light turns off Test alarm by actuating the I O ON OFF switch when the power co...

Page 8: ...he OCSI function In compliance with the ISO 8359 standard The ow supplied is equal to the selected ow accurate to within 10 or 200 ml min whichever is the larger Oxygen Concentration at 2 l min 90 at...

Page 9: ...repairable Electrical power supply Rating 230V 50Hz Average Power 180 W avg Protection Class Class II Mains Protection 5A Filters At the rear of the device a cabinet air lter At the compressor input a...

Page 10: ...blockage Fan is not working Tube disconnected or humidi er cap is not tight Cannula tubing is restricted Observations The I O ON OFF button is in the I ON position but the device does not operate The...

Page 11: ...__________________ ___________________________________________________________________ ___________________________________________________________________ _____________________________________________...

Page 12: ...Drive Birmingham Alabama 35217 U S A Tel 205 856 7200 Fax 205 856 0533 info nidekmedical com www nidekmedical com EU Representative mdi Europa GmbH Langenhagener Str 71 30855 Hannover Langenhagen Ger...

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