50 | Ottobock
11 Legal Information
11.1 Liability
The manufacturer will only assume liability if the product is used in accordance with the descrip
tions and instructions provided in this document. The manufacturer will not assume liability for
damage caused by disregard of this document, particularly due to improper use or unauthorised
modification of the product.
11.2 CE Conformity
This product meets the requirements of the European Directive 93/42/EEC for medical devices.
This product has been classified as a class I device according to the classification criteria out
lined in Annex IX of the directive. The declaration of conformity was therefore created by the man
ufacturer with sole responsibility according to Annex VII of the directive.
12 Technical data
For the technical data, see Figure
35
on page 25.
Abbreviations in the technical data
1
h
s-prox
Proximal system height
2
h
s-dist
Distal system height
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