Ottobock 6A20-10 Instrucciones De Uso página 14

2) The shuttle lock may be unscrewed from the thread by no more
than 3/4 of a turn to align it.
3) Secure the cap screw of the threaded clamping using Loctite®
and tighten using the torque wrench (10 Nm).
Screwing in the ratchet unit
> Required materials: 710D4 torque wrench, attachment for
square drive socket wrench (1/4" inside to 1/2" outside), wrench
socket
► Screw the ratchet unit into the shuttle lock (torque value: 20 Nm).
6 Use
CAUTION
Installation of the pin in a liner that is not approved
Risk of injury due to loosening of the screw connection
► Only install the pin in liners with a metal thread and observe the
specified tightening torque.
CAUTION
Pin not fully inserted into the lock
Risk of injury due to loss of connection to the prosthesis
► Guide the pin into the lock in accordance with the instructions.
► Always verify that the pin is engaged in the lock before using the
prosthesis.
The liner and shuttle lock are connected to each other with the pin.
The pin engages in the shuttle lock and holds the liner in place.
Putting on the Liner
1) Check the pin and liner for damage.
2) NOTICE! Align the pin with the longitudinal axis of the resid­
ual limb to prevent damage.
Roll up the liner and place it on the end of the residual limb.
3) Unroll the liner onto the residual limb so that it has no wrinkles,
without shifting the soft tissue.
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4) Check the fit and the alignment of the liner.
Donning the Prosthetic Socket
1) Slide into the prosthetic socket with the liner until the pin slides
into the opening of the shuttle lock.
2) Insert the pin fully into the shuttle lock.
3) Before using the prosthesis, verify that the pin is fully engaged in
the shuttle lock.
Doffing the Prosthetic Socket
► Press and hold the side button and pull the residual limb with the
liner out of the prosthetic socket.
7 Maintenance
► A visual inspection and functional test of the prosthetic compon­
ents should be performed after the first 30 days of use.
► Inspect the entire prosthesis for wear during normal consulta­
tions.
► Conduct annual safety inspections.
8 Legal information
All legal conditions are subject to the respective national laws of the
country of use and may vary accordingly.
8.1 Liability
The manufacturer will only assume liability if the product is used in
accordance with the descriptions 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.
8.2 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 outlined in Annex IX of
the directive. The declaration of conformity was therefore created by