Otto Bock 757B35-0 Instructions For Use Manual page 21

10 Disposal
This product may not be disposed of with regular domestic waste in all jurisdictions. Dis­
posal that does not comply with the regulations of your country may have a detrimental
impact on health and the environment. Please observe the information provided by the
responsible authorities in your country regarding return and collection processes.
11 Legal Information
11.1 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 com­
bination 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 com­
binations which it did not authorise. The device may only be opened and repaired by authorised
Ottobock technicians.
11.2 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.
11.3 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 the manu­
facturer with sole responsibility according to appendix VII of the guidelines.
12 Appendices
12.1 Symbols on the Battery
Symbol
12.2 Accessories
757VAK1 Battery Adapter Cable for the VASI System
Declaration of conformity according to the European Dir­
ective for Medical Devices 93/42/EEC.
This product must not be disposed of with regular
domestic waste. Disposal that does not comply with the
regulations of your country may have a detrimental
impact on health and the environment. Please note the
information provided by the responsible authorities in
your country regarding return and collection processes.
Lot number
Legal manufacturer
Meaning
Ottobock | 21