Maintenance Instructions; Legal Information - Ottobock 1C60 Triton Gebrauchsanweisung

1. Push on the medial or lateral side of the heel wedge with your finger to free it from the mating
stop (Fig. 3, Pos. 7) on the attachment spring (Fig. 3, Pos. 2).
2. After the heel wedge is partially free grab it by the respective lateral or medial side and pull it
free from the prosthetic foot.
5.4 Foam cover
Both Footshell Connection Caps 2C20 (slim) and 2C19 (normal) serve as a detachable connec-
tion between the foam cover and the footshell. They snap into the proximal brim of the footshell.
1. Cut the foam cover to length, allowing for distal compression about 0.4 in (10 mm) for transtibial
and about 1.6 in (40 mm) for transfemoral covers.
2. With the connection cap attached to the footshell, pull the foam cover over the prosthesis, re-
assemble the foot and mark the outer contours of the connection cap.
3. Remove the connection cap and clean the foam cover with Isopropyl Alcohol 634A58.
4. Apply 636N9 Ottobock Contact Adhesive or 636W17 Plastic Adhesive to the distal end of the
foam cover and to the connection cap.
5. Allow the adhesive to dry (approx. 10 minutes) and cut out a space in the distal foam cover
with a grinding and milling machine to allow for precise fit for the upper part of the adapter.
Sufficient space should be available for the adapter to ensure proper function and eliminate
noise during walking.
6. Assemble the foam cover and finish off the outer shape of the foam cover in usual way with
carbon foot installed. Any compression of the foam cover by cosmetic stockings or SuperSkin
needs to be taken into account.

6 Maintenance instructions

• Foot assembly should be inspected after 30 days (4 weeks) of use.
• Inspection of the entire prosthesis for wear during normal consultations.
• Footshell may require replacement if wear is excessive.

7 Legal information

All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.
7.1 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 disregard of this document, particularly due to improper use or unauthorised
modification of the product.
7.2 CE conformity
This product meets the requirements of the European Directive 93 / 42 / EEC for medical devices.
This product has been classified as a class I device according to the classification criteria outlined
in Annex IX of the directive. The declaration of conformity was therefore created by the manufac-
turer with sole responsibility according to Annex VII of the directive.
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