Symbols; Product Specifications - CMF SPINALOGIC Patientenhandbuch

Symbols

EQUIPMENT SAFETY ELECTRIC SHOCK
CLASSIFICATION TYPE BF APPLIED PART
CAUTION, CONSULT ACCOMPANYING
DOCUMENTS
MANUFACTURER
TEMPERATURE LIMITATIONS
ELECTRICAL AND ELECTRONIC EQUIPMENT
(EUROPE)
Warranty
It is DJO, LLC policy that all complaints about our devices be
communicated to Customer Care at 800-263-6004. The Customer
Service Representative will provide technical assistance to determine
the extent of the problem or educate the patient on the use of the
device. If the device cannot be made to function properly, a
replacement device is sent to the patient free of charge and the
malfunctioning device is brought back for testing and evaluation. This
procedure can be done at any time, and as many times as necessary,
during the course of treatment. The course of treatment is defined as
the nine (9) month period between the time the device is initiated and
the Two Hundredth and Seventieth (270th) treatment.
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Product Specifications

Manufacturer DJO, LLC
1430 Decision Street
Vista, CA 92081-8553 U.S.A.
Model Type SpinaLogic®
Operating Temperature +50°F (10°C) to +100°F (38°C)
Range
Note: CMF Bone Growth Stimulators must remain at Operating
Temperature one hour prior to use
Storage and
+5°F (-15°C) to +140°F (60°C)
Transportation
Temperature Range
Operating Humidity Range
Maximum 85% Relative Humidity
Dimensions 11 in x 12 in x 1.5 in (28 cm x 31 cm x 4 cm)
Weight 2.0 lbs (0.9 kg)
Equipment not suitable for use in the presence of a flammable anaesthetic mixture with
air or with oxygen or nitrous oxide
Degree of Protection Ordinary Equipment
Against Ingress of Liquids
Degree of Protection TYPE BF Applied Part
Against Electric Shock
Power Supply Battery Operated, Replaceable, 9 Volts Direct Current
Short time continuous operation, 30 minutes per day
Mode of Operation
Electromagnetic
This products is in conformity with Directive 89/336/EEC
Compatibility (EMC)
Electromagnetic Immunity
(EMI)
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