Ottobock C-Leg Serie Información Para El Usuario página 38

Liability
The device is only to be used under the specified conditions and for the intended purposes. The device must
be maintained according to the Instructions for Use. The device must only be operated with tested modular
components in accordance with the Otto Bock Mobility System. The manufacturer is not liable for damage
caused by component combinations that were not authorized by the manufacturer.
The C-Leg prosthesis system is designed exclusively for use on one patient. Use of the product by a further
person is not approved by the manufacturer.
Trademarks
All denotations within this accompanying document are subject to the provisions of the respective applicable
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.
CE Conformity
The electronic 3C88-2 / 3C98-2 C-Leg Prosthesis System meets the requirements of the 93 / 42 / EEC guide-
lines for medical devices. This product 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 Otto
Bock with sole responsibility according to appendix VII of the guidelines.
The electronic 3C88-2 / 3C98-2 C-Leg Prosthesis System also meets the requirements of the 1999 / 5 / EC
guidelines for radio equipment and telecommunications terminal equipment. Conformity assessment was
carried out by Otto Bock according to appendix IV of the guidelines. A copy of the declaration of conformity
can be requested from the manufacturer (see back side).
38 | Ottobock C‑Leg