Ottobock 8359 Genu Direxa Stable Instrucciones De Uso página 13

7) The two wide hook-and-loop closures at the rear may only be adjusted and fastened by quali­
fied personnel (see Fig. 7, item 3 and item 4).
8) Fasten the lower front hook-and-loop closure (see Fig. 7, item 5).
9) Fasten the upper front hook-and-loop closure (see Fig. 7, item 6).
10) The two hook-and-loop closures at the rear may only be adjusted and fastened by qualified
personnel (see Fig. 7, item 7 and item 8, and see Fig. 3). Optional: For the corresponding
indication, fasten the hook-and-loop closures crosswise (see Fig. 4).
4.3 Cleaning
NOTICE
Use of improper cleaning agents
Damage to the product due to use of improper cleaning agents
► Only clean the product with the approved cleaning agents.
1) Pull the black strap upwards to remove the bracket over the joint bar (see Fig. 8).
2) Pull the joint bars out of the orthosis (see Fig. 9).
3) Fasten all hook-and-loop closures.
4) Recommendation: Use a laundry bag or net.
5) Wash the orthosis in warm water at 40 °C with standard mild detergent. Do not use fabric
softener. Rinse thoroughly.
6) Allow to air dry. Do not expose to direct heat sources (e.g. sunlight, stove or radiator).
7) Reinsert the joint bars.
INFORMATION: The labelling on the joint bars must be visible from the outside.
8) Pull the black strap first upwards and then downwards to position the bracket over the joint
bar.
5 Disposal
Dispose of the product in accordance with national regulations.
6 Legal Information
All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.
6.1 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.
6.2 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 out­
lined in Annex IX of the directive. The declaration of conformity was therefore created by the man­
ufacturer with sole responsibility according to Annex VII of the directive.
1 Avant-propos
INFORMATION
Date de la dernière mise à jour : 2014-07-29
► Veuillez lire attentivement l'intégralité de ce document.
► Respectez les consignes de sécurité.
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