6 Maintenance
INFORMATION
The product may be exposed to increased loads by the patient.
► Shorten the maintenance intervals according to the expected loads.
The manufacturer recommends a semi-annual inspection to verify functional
ity and check for wear of the system joints.
Follow the maintenance schedule included with the E-MAG instructions for
use.
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 accord
ance with the descriptions 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 class I accessories
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
INFORMATION
Date de la dernière mise à jour : 2016-01-29
► Veuillez lire attentivement l'intégralité de ce document avant d'utiliser le
produit.
► Respectez les consignes de sécurité afin d'éviter toute blessure et en
dommagement du produit.
► Apprenez à l'utilisateur à bien utiliser son produit et informez-le des
consignes de sécurité.
► Conservez ce document.
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