Maintenance/Repair; Service Information; Legal Information; Trademarks - Ottobock AxonRotation Instrucciones De Uso

CAUTION
Disconnecting or establishing electrical connections when switched on
► Injury due to faulty control or malfunction of the Axon-Bus prosthethic system.
→ Power down the Axon-Bus prosthethic system by pressing the button in the charging recept­
acle before changing any Axon-Bus components (e.g. Axon-Bus gripping component).
8 Cleaning
1) Clean the product with a damp cloth and mild soap (e.g. Ottobock 453H10=1 Derma Clean)
when needed.
Ensure that no liquid penetrates into the system component(s).
2) Dry the product with a lint-free cloth and allow it to air dry fully.

9 Maintenance/Repair

9.1 Service Information

Since all moving mechanical parts are subject to wear and tear, regular service is required within
the guarantee period. In the course of service, Ottobock Service (Ottobock Myo-Service) checks
the entire product. Wear parts are replaced as required. Omitting a scheduled service inspection
voids the guarantee.

10 Legal Information

10.1 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.

10.2 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 justi­
fy the conclusion that the denotation in question is free of third-party rights.
10.3 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.
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