with components that were authorised by the manufacturer (see instructions
for use and catalogues). The manufacturer does not assume liability for dam
age caused by component combinations which it did not authorise. The
device may only be opened and repaired by authorised Ottobock techni
cians.
9.2 CE Conformity
This device meets the requirements of the 93 / 42 / EEC guidelines for med
ical 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 appendix VII of the guidelines.
9.3 Trademarks
All denotations within this accompanying document are subject to the provi
sions 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 identi
fied as such, this does not justify the conclusion that the denotation in ques
tion is free of third-party rights.
1 Caractère actuel des instructions d'utilisation
INFORMATION
Date de la dernière mise à jour : 2013-01-22
► Veuillez lire attentivement l'intégralité de ce document.
► Respectez les consignes de sécurité.
2 Description du produit
2.1 Description
L'interrupteur à bascule 9X25 est conçu pour être monté sur l'emboîture dé
finitive. L'interrupteur à bascule 9X25 est conçu pour des patients qui ne
parviennent pas à produire un signal musculaire leur permettant de com
mander les prothèses myoélectriques, mais qui veulent pourtant profiter du
potentiel élevé de rééducation que présentent ces prothèses.
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