Otto Bock 3B5-X2, Инструкция по эксплуатации

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Storage
• When storing the knee joint, press the top of the knee to the flexion stop.
• Avoid extended disuse of the product (use the product regularly).
13 Cleaning
1) Clean the product with a damp cloth (fresh water) when needed.
2) Dry the product with a lint-free cloth and allow it to air dry fully.
14 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 maintenance (service inspections) is mandatory in the interest of one's safety and in
order to maintain operating reliability and protect the warranty. This maintenance includes 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.
15 Legal information
All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.
15.1 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.
15.2 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.
15.3 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.