Ottobock 12K19 Gebrauchsanweisung Seite 15

• Once again, temporarily affix the wrist unit and terminal device to the
elbow set-up to verify the length of the prosthesis. Shorten the forearm
socket a bit more, if necessary. It is important, however, that the diameter
for the wrist unit remains unchanged in the forearm socket.
4.2.2 12K19=40
Disassembling the Lamination Ring (12K19=40)
• After loosening the 506G1=M8x15 Adjustment Screws (Fig. 2, item A),
the lamination ring with 13G9=47 Upper Arm Rotation Piece (Fig. 2,
item B) can be separated from the elbow ball.
Assembly
Refer to Assembly of 12K5=* / 12K20=* (Section 4.2.1).
5 Liability
Otto Bock Healthcare GmbH, hereafter referred to as manufacturer, as-
sumes liability only if the user complies with the processing, operating and
maintenance instructions as well as the service intervals. The manufacturer
explicitly states that this device may only be used in combination with com-
ponents that were authorised by the manufacturer (see instructions for use
and catalogues). The manufacturer does not assume liability for damage
caused by component combinations which it did not authorise.
The device may only be opened and repaired by authorised Ottobock
technicians.
6 CE Conformity
This device meets the requirements of the 93 / 42 / EEC guidelines for medi-
cal devices. This device has been classified as a class I device according
to the classification criteria outlined in appendix IX of the guidelines. The
declaration of conformity was therefore created by Ottobock with sole
responsibility according to appendix VII of the guidelines.
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