Product Specifictions - CMF OL1000 Instructions D'utilisation

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Product Specifictions

Manufacturer
Model Types
Operating Conditions
Transport and Storage
Conditions
Dimensions
Weight
Equipment not suitable for use in the presence of a flammable anaesthetic mixture with air or
with oxygen or nitrous oxide .
Degree of Protection Against
Ingress of Liquids
Degree of Protection Against
Electric Shock
Power Supply
Mode of Operation
Electromagnetic Compatibility
(EMC) Electromagnetic
Immunity (EMI)
No effect from lint, dust, light .
This device is not intended for use in an Oxygen Rich Environment .
Degree of Protection against Electric Shock: internally powered ME equipment .
Expected Service Life is 270 days from initial use .
Expected shelf life is 2 .5 years .
No Sterilization is required .
26
DJO, LLC • 1430 Decision Street
Vista, CA 92081-8553 U .S .A .
OL1000 & OL1000 SC
Temperatures: +41°F (5°C) to +10°F (40°C)
Relative Humidity: 15% to 93% non-condensing
Atmospheric Pressure: 700hPa to 1060 hPa
Altitude: Maximum of 3000m
NOTE: CMF Bone Growth Stimulators must remain at
Operating Temperature one hour prior to use .
Temperatures: -13°F (-25°C ) without relative humidity con-
trol, up to 158°F (70°C)
Relative Humidity: 15% - 93% non-condensing
Atmospheric Pressure: 500 hPa to 1060 hPa
11 in x 12 in x 1 .5 in (28 cm x 31 cm x 4 cm)
2 .0 lbs (0 .9 kg)
IP22 . Protected against solid foreign objects of 12 .5mm
dia and greater . Protected against vertically falling water
drops when enclosure tilted up to 15° .
TYPE BF Applied Part
Battery operated, replaceable, 9 volts direct current .
Battery operated device (9V standard battery), not to use
lithium batteries .
Short time continuous operation, 30 minutes per day
These products are in conformity with Directive 89/336/
EEC .