Streifeneder ortho.production GO.relax 5A420 Serie Instrucciones De Uso página 10

Assembly
„
Always make sure to put on the Spectra sock before assembling the cosmetic foot
cover.
Firmly push the foot into the cosmetic cover. Ensure that the heel makes contact on the edge
of the cosmetic cover (Fig. 5, similar).
To make donning the cosmetic foot cover easier, insert the long end of the shoe horn along
the side underneath the heel. Then lever the foot into the cosmetic cover on a table edge
(Fig. 6, similar).
Optional water drainage opening
„
Before drilling the optional water drainage opening, make sure that the prosthetic foot
and Spectra sock were removed from the cosmetic foot cover.
There is an area with a thinner wall on the underside of the cosmetic foot cover. A water drainage
opening with a diameter of 6 mm can be cut or drilled here if necessary (Fig. 7 and 8).
It is essential to ensure that the product is not exposed to chemicals and substances
such as salt water, acids, dust or sand!
The corrosion resistance of this product is limited and depends on the component with
the lowest corrosion resistance used in the prosthesis structure, which determines the
maximum corrosion resistance of the entire structure.
The prosthesis must be rinsed thoroughly with fresh water every time it comes
into contact with water. After rinsing, the prosthesis should be dried.
Failure to observe these instructions will make any claims against Streifeneder
ortho.production GmbH null and void.
Please inform your patient accordingly!
Maintenance and Service
„
The prosthetic foot is maintenance-free.
In the event of malfunctions, the product must be sent in.
Please note that repairs to the product may be carried out only by Streifeneder
ortho.production GmbH.
In general, the entire prosthesis should be inspected for wear every 6 months.
If necessary, replace the cosmetic foot cover and/or Spectra sock.
Declaration of Conformity
„
Streifeneder ortho.production GmbH declares as manufacturer with sole responsibility that the
product complies with Regulation (EU) 2017/745 for medical devices (MDR).
10/20