2) Dry the orthosis joint with a cloth or allow it to air-dry. Avoid exposure to
direct heat (e.g. from an oven or radiator).
7 Maintenance
INFORMATION
The product may be exposed to increased loads by the patient.
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Shorten the maintenance intervals according to the expected loads.
The manufacturer recommends a semi-annual inspection to verify functional
ity and check for wear and tear to the orthotic joints.
Spare parts are listed in the section "Components/design".
8 Disposal
Dispose of the product in accordance with national regulations.
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 accord
ance 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 unauthor
ised modification of the product.
9.2 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 manufacturer
with sole responsibility according to Annex VII of the directive.
1 Avant-propos
Français
INFORMATION
Date de la dernière mise à jour : 2019-08-05
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Veuillez lire attentivement l’intégralité de ce document avant d’utiliser le
produit.
15
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