Safety instructions and warnings
18/82
The manufacturer is obliged to take back and dispose of certain electrical and
electronic components in accordance with the 2012/19/EC Directive.
The components and devices are labelled with the following symbol:
The device will, if requested, be properly disposed of by the JK Corporate
Group. This service is available free of charge. Your partner agency or dealer
will be happy to advise.
Registration numbers
Companies within the JK Corporate Group are registered as manufacturers in
Germany and accept all obligations in respect of the German Electrical and
Electronic Equipment Act.
Registry number JK-Products GmbH (Devices):
WEEE-DE 62655951
1.5.10
Directives
This device was built according to the following guidelines:
EU directive for medical products 93/42/EEC (according to the version
valid at the time).
1.5.11
Export
We emphasize that these devices are only intended for the European market
and must not be exported to or operated in other countries e.g. the USA or
Canada! The manufacturer does not accept any liability in the event of non-
observance! We explicitly emphasize that non-compliance may result in high
liability risks for the exporter and/or the operator.
1.5.12
Technical modifications
The device has been constructed in accordance with the current state-of-the-
art and the applicable safety regulations. The illustrations and specifications
on these instructions are subject to technical modifications which are required
in order to improve the device.
Unauthorized modifications and changes to the device and its control unit are
prohibited. Failure to comply with this voids the operating licence!
Please use only original spare parts. Any liability for damage or injury proven
to be the result of the use of non-genuine spare parts is excluded.
