Ottobock 1K10 Instructions D'utilisation page 8

5.2 Alignment
NOTICE
Grinding the prosthetic foot
Premature wear resulting from damage to the prosthetic foot
► Do not grind the prosthetic foot.
5.2.1 Bench Alignment
Foot size Mid-foot anterior to the
alignment reference line
12 – 16 cm
17 – 21 cm
5.2.2 Static Alignment
• Ottobock recommends checking the alignment of the prosthesis
using the L.A.S.A.R. Posture and adapting it as needed.
• If necessary, the alignment recommendations (TF modular leg
prostheses: 646F219*, TT modular leg prostheses: 646F336*)
may be requested from Ottobock.
5.2.3 Dynamic Trial Fitting
• Adapt the alignment of the prosthesis in the frontal plane and the
sagittal plane (e.g. by making angle or slide adjustments) to
ensure an optimum gait pattern.
TT fittings: Make sure that physiological knee movement in the
•
sagittal and frontal plane is achieved when the leg begins to bear
weight after the heel strike. Avoid medial movement of the knee
joint. If the knee joint moves in the medial direction in the first half
of the stance phase, move the prosthetic foot in the medial direc­
tion. If the medial movement occurs in the second half of the
stance phase, reduce the exterior rotation of the prosthetic foot.
6 Cleaning and Care
1) Clean the product with a damp, soft cloth.
2) Dry the product with a soft cloth.
3) Allow to air dry in order to remove residual moisture.
8
Heel height
15 mm see Technical
Data
20 mm
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.
► Have the prosthetic components inspected every 3 months.
8 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.
9 Legal information
All legal conditions are subject to the respective national laws of the
country of use and may vary accordingly.
9.1 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.
9.2 CE conformity
The product meets the requirements of Regulation (EU) 2017/745 on
medical devices. The CE declaration of conformity can be down­
loaded from the manufacturer's website.
10 Technical data
Reference number
Heel height [mm]
Colours
1K10 1K30 1S30
5 ± 5 5 ± 5 10 ± 5
Beige