Local Legal Information - Ottobock Axon-Bus Instrucciones De Uso

8 Cleaning
NOTICE
Improper product care
Damage to the product due to the use of incorrect cleaning agents.
Only clean the product with a damp cloth and mild soap (e.g. 453H10=1 Ottobock Der­
►
maClean).
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
► Inspect the entire prosthesis for wear during normal consultations.
9.1 Service
Since all moving mechanical components are subject to wear and tear, regular service is required
within the guarantee period. The entire product is inspected by Ottobock Service (Ottobock Myo-
Service). Wear parts are replaced as required.
Failure to adhere to the service schedule invalidates the warranty.
10 Legal information
All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.
10.1 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.
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.
This product meets the requirements of the European Directive 1999/5/EC for radio equipment
and telecommunications terminal equipment. The conformity assessment was drawn up by the
manufacturer in accordance with Annex IV of the directive.

10.4 Local Legal Information

Legal information that applies exclusively to specific countries is written in the official language
of the respective country of use in this chapter.
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