Ottobock 1M10 Adjust Instructions D'utilisation page 14

There is a connecting element (such as a connection plate, connection cap or connection cover)
on the prosthetic foot.
Required materials: degreasing cleaner (e.g. 634A58 isopropyl alcohol), 636N9 contact
>
adhesive or 636W17 plastic adhesive
1) Measure the length of the foam cover on the prosthesis and add the length allowance.
TT prostheses: Distal allowance for movement of the prosthetic foot.
TF prostheses: Allowance proximal of the knee rotation point for flexion of the prosthetic knee
joint and distal allowance for movement of the prosthetic foot.
2) Cut the pre-shaped foam cover to length and fit it in the proximal area on the prosthetic sock­
et.
3) Pull the foam cover over the prosthesis.
4) Set the connecting element onto the footshell or prosthetic foot. Depending on the version,
the connecting element engages in the edge or rests on the foot adapter.
5) Install the prosthetic foot on the prosthesis.
6) Mark the outer contour of the connecting element on the distal face of the foam cover.
7) Disassemble the prosthetic foot and remove the connecting element.
8) Clean the connecting element using a degreasing cleaner.
9) Glue the connecting element onto the distal face of the foam cover according to the marked
outer contour.
10) Let the glue dry (approx. 10 minutes).
11) Install the prosthetic foot and adapt the exterior cosmetic shape. Take into account compres­
sion caused by cosmetic stockings or SuperSkin.
6 Maintenance
► A visual inspection and functional test of the prosthetic components should be performed
after the first 30 days of use.
► Inspect the entire prosthesis for wear during normal consultations.
► Conduct annual safety inspections.
7 Disposal
In some jurisdictions it is not permissible to dispose of the product with unsorted household
waste. Improper disposal can be harmful to health and the environment. Observe the information
provided by the responsible authorities in your country regarding return, collection and disposal
procedures.
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 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.
8.2 CE conformity
The product meets the requirements of Regulation (EU) 2017/745 on medical devices. The CE
declaration of conformity can be downloaded from the manufacturer's website.
9 Technical data
Sizes [cm]
Heel height with 2C1=*N [mm]
14
22 23 24 25 26 27 28
10 ±5
29 30