pletely. When the hydraulic unit cools down, the product switches back to the settings that exis
ted before the overheating mode.
Overheating mode is indicated by a brief vibration every 5 seconds.
10 Cleaning
1) Switch off the product before cleaning.
2) Clean the product with a damp cloth and mild soap when needed.
Make sure that no liquids get into the product and product components.
3) Dry the product with a lint-free cloth and allow it to air dry fully.
11 Maintenance
INFORMATION
The foot shell for the prosthetic foot has an expected working life of approx. one year when pro
fessionally mounted and properly used. Damaged foot shells must be replaced immediately,
before the prosthetic foot is used again.
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
inspecting the sensors and replacing wear and tear parts.
When maintenance (a service inspection) is due, this is indicated after the service interval has
expired by three brief beeps after disconnecting the battery charger. Please contact your O&P
professional for more information.
To have a service inspection carried out, please submit the product as well as the battery charger
and power supply unit to the prosthetist.
12 Legal information
All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.
12.1 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.
12.2 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.
12.3 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
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