Legal Information; Liability; Trademarks; Ce Conformity - Ottobock Genium X3 3B5-3 Gebrauchsanweisung

The duration of use can be individually extended depending on the intensity of use by perform­
ing regular service inspections.
Regular service inspections (maintenance) are mandatory in the interest of your 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 wear and tear parts.
If maintenance is due, this is indicated after the service interval has expired by three brief beep
and vibration signals after disconnecting the battery charger. For further information, please con­
tact your O&P professional.
To have a service inspection carried out, please submit the product as well as the battery charger
and power supply unit to the prosthetist.

14 Legal information

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

14.1 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 disregarding the information in this document, particularly due to improper
use or unauthorised modification of the product.

14.2 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.

14.3 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.
Hereby, Ottobock Healthcare Products GmbH declares that the product is in compliance with
Directive 2014/53/EU. The full text of the EU declaration of conformity is available at the following
internet address: www.ottobock.com/conformity
The product meets the requirements under the RoHS Directive 2011/65/EU of the European Par­
liament and of the Council of 8 June 2011 on the restriction of the use of certain hazardous sub­
stances in electrical and electronic equipment.

14.4 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.
This device complies with part 15 of the FCC Rules. Operation is subject to the following two
conditions:
1) This device may not cause harmful interference, and
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