can obtain information about known risks and the current
options for refurbishing the product.
10.2 Liability
The manufacturer will only assume liability if the product is
used in accordance with the descriptions and instructions
provided in this document. The manufacturer will not
assume liability for damage caused by disregard of this doc
ument, particularly due to improper use or unauthorised
modification of the product.
10.3 CE Conformity
This product meets the requirements of the European Dir
ective 93/42/EEC for medical devices. This product has
been classified as a class I device according to the classific
ation criteria outlined 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.
The product meets the requirements under the RoHS Dir
ective 2011/65/EU of the European Parliament and of the
Council of 8 June 2011 on the restriction of the use of cer
tain hazardous substances in electrical and electronic equip
ment.
10.4 Warranty
Further information on the warranty terms and conditions is
available from the manufacturer's service (see inside back
cover for addresses).
C1000 SF
10.5 Trademarks
All product names mentioned in this document are subject
without restriction to the respective applicable trademark
laws and are the property of the respective owners.
All brands, trade names or company names may be
registered trademarks and are the property of the respective
owners.
Should trademarks used in this 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.
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