Ottobock 15K10 Gebrauchsanweisung Seite 7

15K10 modular foam kit
Fig. Item Quant­
ity
1 – 1( )
1 – 1( )
1 – 1( )
5 Preparing the product for use
5.1 Preparation
> The modular prosthesis has been prepared.
1) INFORMATION: In both areas, add an allowance of 2 to 3 cm
for compression.
Forearm area: determine the length of the prosthesis from the
terminal device to the modular elbow joint.
Upper arm area: determine the length of the prosthesis from the
modular elbow joint to the prosthesis socket/prosthetic shoulder
joint.
2) Determine the circumferences on the contralateral side. For a
bilateral fitting, pay attention to the overall aesthetic impression.
3) Cut the foam moulded parts to length.
5.2 Assembling
Materials needed: 636W17 plastic adhesive, 13R9* connection
>
disc with groove (for connection with a wrist), 13R8=64 connec­
tion flange (for connection to the lamination ring), 623T8=9 Perlon
frizz stockinette
1) Bond the required connection components to the moulded foam
parts with plastic adhesive.
2) Push the moulded foam parts onto the modular prosthesis.
3) Optional: Bond the moulded foam parts to each other.
4) Grind the contour of the cosmetic foam cover.
5) Pull a double layer of Perlon frizz stockinette over the cosmetic
foam cover and secure it to the connection disc.
Designation Reference
number
Upper arm moulded –
foam part
Perlon frizz stockinette –
Mounting flange 13R8=64
6 Cleaning
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.
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 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) 2017/745on
medical devices. The CE declaration of conformity can be down­
loaded from the manufacturer's website.
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