Legal Information - Ottobock 6A40 MagnoFlex Lock Gebrauchsanweisung

> Required tools and materials:
Torque Wrench (adjustable to 3 Nm), 636K13 Loctite
®
1) Apply Loctite to the thread.
2) NOTICE! Do not shorten the pin.
Screw the pin into the thread and tighten it (see fig. 16) (tighten­
ing torque: 3 Nm).
6 Use
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. The pin must be flexible and
always spring back to the original position.
2) NOTICE! Misaligning the pin leads to damage during inser­
tion in the shuttle lock.
Apply the liner on the end of the residual limb so that the pin is
aligned with the longitudinal axis of the residual limb.
3) Roll the liner over the residual limb.
4) Check the fit of the liner and the alignment of the pin.
Donning the Prosthetic Socket
1) With the liner, slide into the prosthetic socket until the pin slides
into the opening of the lamination adapter.
2) INFORMATION: While the pin is being inserted, clicking
®
noises caused by the magnet and the ratchet unit can be
heard. These noises do not indicate whether the pin is fully
engaged in the ratchet unit.
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
The product meets the requirements of Regulation (EU) 2017/745 o n
medical devices. The CE declaration of conformity can be down­
loaded from the manufacturer's website.
17