Ottobock 8E38 Patienteninformation Seite 10

5 Liability
Otto Bock Healthcare Products GmbH, hereafter referred to as manufacturer, assumes liability only if the user
complies with the processing, operating and maintenance instructions as well as the service intervals. The
manufacturer explicitly states that this device may only be used in combination with components that were
authorised by the manufacturer (see instructions for use and catalogues). The manufacturer does not assume
liability for damage caused by component combinations which it did not authorise.
The device may only be opened and repaired by authorised Ottobock technicians.
6 CE Conformity
This device meets the requirements of the 93 / 42 / EEC guidelines for medical devices. This device has been
classified as a class I device according to the classification criteria outlined in appendix IX of the guidelines.
The declaration of conformity was therefore created by Ottobock with sole responsibility according to ap-
pendix VII of the guidelines.
7 Trademarks
All denotations within this accompanying document are subject to the provisions of the respectiveapplicable
trademark laws and the rights of the respective owners, with no restrictions.
All brands, trade names or company names may be 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 conclusion that the denotation in question is free of third-party rights.
10 | Ottobock