Ce Conformity - Otto Bock B400 Instructions For Use Manual

Legal Information
described. The manufacturer recommends that the device
be used and maintained according to the instructions for
use.
The manufacturer is not responsible for damages caused by
components and spare parts not approved by the manufac­
turer. Repairs must be carried out exclusively by authorised
dealers or by the manufacturer.

10.2 CE Conformity

This device meets the requirements of the 93 / 42 / EEC
guidelines for medical devices. This device has been classi­
fied as a class I device according to the classification criter­
ia outlined in appendix IX of the guidelines. The declaration
of conformity was therefore created by the manufacturer
with sole responsibility according to appendix VII of the
guidelines.
10.3 Warranty Terms and Conditions
Further information on the warranty terms and conditions is
available from the manufacturer's service (see inside back
cover for addresses).
10.4 Trademarks
All denotations within this accompanying document are sub­
ject to the provisions of the respective applicable trademark
laws and the rights of the respective owners, with no restric­
tions.
All brands, trade names or company names may be
18 | Ottobock
registered trademarks and are subject to the rights of the
respective owners.
Should trademarks in this accompanying document fail to be
explicitly identified as such, this does not justify the conclu­
sion that the denotation in question is free of third-party
rights.
B400