Compex full fitness, User Manual

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English
165
4. Maintenance
T
o clean your unit, use a soft duster
and an alcohol-based cleaning pro-
duct, which does not contain any sol-
vents. In fact, solvents could damage
the plastic parts, especially the panel
covering the screen of your Compex.
T
he user must not attempt any re-
pairs to the device or any of its acces-
sories. Never dismantle the Compex
or the charger containing high-vol-
tage parts because of risk of electric
discharge.
C
ompex Médical SA declines all
responsibility for damages and
consequences resulting from any
attempt to open, modify or repair the
device or any of its components by a
person or a service centre not
officially approved by Compex
Médical SA.
C
ompex stimulators do not require
calibration or verification of perfor-
mance parameters. The characteris-
tics are systematically verified and
validated for each device manufactu-
red. These characteristics are stable
and do not vary when used under
normal conditions.
I
f your device seems to not function
as expected, regardless of the situa-
tion, contact an official Compex ser-
vice centre for assistance.
M
edical and health professionals
must refer to local legislation for in-
formation related to maintenance.
Normally, these laws require verifica-
tion of certain criteria at regular inter-
vals.
5. Storage conditions
T
he Compex contains rechargeable
batteries and so the storage condi-
tions must not exceed the following
figures:
TempérStorage temperature from -20°C to 45°
Max. relative humidity 75%
Atmospheric pressure from 700 hPa to
1060 hPa
6. Use conditions
Temperature of use from 0°C to 40°C
Max. relative humidity from 30% to 75%
Atmospheric pressure from 700 hPa
to1060 hPa
Do not use in an explosion risk area.
7. Elimination
F
or environmental protection and ac-
cording to the country's national re-
quirements, the device, the battery
and the accessories have to be elimi-
nated with special waste.
8. Standards
T
he Compex is based directly on me-
dical technology.
T
o guarantee your safety, the design,
manufacturing and distribution of
Compex are in conformity with the
requirements of the European Direc-
tive 93/42/CEE.
T
he device is in conformity with the
standard for general safety rules for
electromedical devices IEC 60601-1,
the standard for electromagnetic
compatibility IEC 60601-1-2 and the
standard for special safety rules for
nerve and muscle stimulators IEC
60601-2-10.
C
urrent international standards (IEC
60601-2-10 AM1 2001) require that a
warning be given concerning the ap-
plication of electrodes to the thorax
(increased risk of cardiac fibrillation).
Manuel Full Fitness:Full Fitness 0706 5/02/08 10:10 Page 165