Miscellaneous - Medisana BOB Manual

GB
3 Operating / 4 Miscellaneous
3.4
Automatic
switch-off

4 Miscellaneous

4.1
Cleaning and
maintenance
4.2
Disposal
4.3
Directives /
norms
18
Without any button pressed during approx. 2 minutes in the program
select mode, the device will automatically switch off.
The device constantly checks for proper skin contact during the use. If
the unit should detect non-sufficient contact to skin, the pulse emission
will be stopped and the program select mode will be entered.
•
Remove the batteries before you clean the unit.
•
Never use strong cleaning agents or stiff brushes.
•
Clean the unit with a soft cloth which has been lightly moistened with a
mild soap. Never dip the unit into water for cleaning and ensure that no
water gets into the unit at any time. Only use the unit again, when it is
fully dry.
•
Check before each use, if the two round electrode attachments on the
backside of the belt are clean and without obvious defects. In case of
doubt, do not use the device and contact the service centre.
•
Servicing and safety inspection (applies to commercial use):
The unit has been adjusted by the manufacturer for a period of two
years' use. In the case of commercial use, the unit must be serviced
and safety inspected at least once every two years. This inspection will
be charged for and can be carried out by an appropriate authority or an
authorised service centre - in accordance with the regulations for users
of medical equipment.
CAUTION
Do not allow water to penetrate the device.
•
Store the unit in a cool, dry place.
This product must not be disposed of together with domestic waste. All
users are obliged to hand in all electrical or electronic devices, regardless
of whether or not they contain toxic substances, at a municipal or commer-
cial collection point so that they can be disposed of in an environmentally
acceptable manner.
Please remove the batteries before disposing of the device/unit. Do not
dispose of old batteries with your household waste, but at a battery
collection station at a recycling site or in a shop. Consult your municipal
authority or your dealer for information about disposal.
This device meets the requirements of the EU standard for nerve- and
muscle stimulation devices. It is certified in accordance with EC Guidelines
and carries the CE symbol (conformity symbol) "CE 0297". The EMS-device
corresponds to European standards EN 60601-1, EN 60601-1-2 and EN
60601-2-10. The specifications of EU Guideline "93/42/EEC of the Council
Directive dated 14 June 1993 concerning medical devices" are met.
Electromagnetic compatibility:
The device complies with the EN60601-1-2 standard for electromagnetic
compatibility. You can find details on this measurement data on the
MEDISANA homepage www.medisana.com.
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