Cleaning; Maintenance; Legal Information; Liability - Ottobock Genium 3B1-2 Instrucciones De Uso

11 Cleaning

1) Clean the product with a damp cloth and mild soap (e.g. Ottobock 453H10=1 Derma Clean)
when needed.
2) Dry the product with a lint-free cloth and allow it to air dry fully.

12 Maintenance

INFORMATION
This component was tested for three million load cycles in accordance with ISO 10328.
Depending on the activity level, this corresponds to a service life of three to five years.
The duration of use can be individually extended depending on the intensity of use by perform­
ing regular service inspections.
Regular service inspections are recommended in the interest of the user's own safety, and in
order to maintain operating reliability and protect the warranty. These service inspections include
an inspection of the sensors and replacement of worn parts.
To have a service inspection carried out, please submit the product as well as the battery charger
and power supply unit to the prosthetist.
INFORMATION
If a remote control was included in the scope of delivery as an optional product accessory, it
must also be sent along with the product for service inspections.

13 Legal Information

All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.

13.1 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.

13.2 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.

13.3 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 III of the directive.

13.4 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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