Symbols On The Product - Otto Bock DynamicArm 12K100N Patient Information

7 Symbols on the product

Declaration of conformity according to the applicable European directives
This product may not be disposed of with regular domestic waste. Disposal that is not in
accordance with the regulations of your country may have a detrimental impact on health
and the environment. Please note the information provided by the responsible authorities in
your country regarding return and collection processes.
Compliance with the requirements according to "FCC Part 15" (USA)�
Non-ionising radiation�
Compliance with the requirements according to the "Radiocommunications Act" (AUS)�
Legal manufacturer�
Serial number of the device�
8 Liability
Otto Bock Healthcare Products GmbH, hereinafter called manufacturer, assumes liability only if the user observes
the product's specified fabrication and use instructions, adheres to its care instructions, and follows its service
schedule. This product may only be used in combination with components that have been authorised by the manu-
facturer (please refer to the instructions for use and catalogues). The manufacturer assumes no liability for dam-
age caused by component combinations (use of third-party products) and applications which it did not authorise.
This product may only be opened and repaired by authorised Ottobock staff.
9 Trademarks
All product names mentioned in this accompanying document are subject without restriction to the respec-
tive applicable trademark laws and 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 accompanying document fail to be explicitly identified as
such, this does not justify the conclusion that the denotation in question is free of third-party rights.
10 CE conformity
This device meets the requirements of Directive 93/42/EEC for medical devices. This product has been
classified as a class I device according to the classification criteria outlined in appendix IX of the directive.
The manufacturer therefore drew up the declaration of conformity under its own responsibility according to
appendix VII of the directive.
This device also meets the requirements of Directive 1999/5/EC for radio equipment and telecommunications
terminal equipment. The declaration of conformity was created by the manufacturer according to Appendix III of
the directive. A copy of the declaration of conformity can be requested from the manufacturer (see last page).
20 | Ottobock DynamicArm 12K100N / DynamicArm Plus 12K110N