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 disregard of this
document, particularly due to improper use or unauthorised modification of
the product.
9.2 CE Conformity
This product meets the requirements of the European Directive 93 / 42 / E EC
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.
9.3 Warranty
The manufacturer warrants this device from the date of purchase. The war
ranty covers defects that can be proven to be a direct result of flaws in the
material, production or construction and that are reported to the manufac
turer within the warranty period.
Further information on the warranty terms and conditions can be obtained
from the competent manufacturer distribution company.
10 Technical data
Reference number
Weight [g]
System height [mm]
Material
Max. body weight [kg]
1 Description du produit
INFORMATION
Date de la dernière mise à jour : 2014-08-19
► Veuillez lire attentivement l'intégralité de ce document.
► Respectez les consignes de sécurité.
1.1 Conception et fonctionnement
Les ancres à couler 4R111, 4R111=N et 4R116=T se montent par stratifica
tion dans une emboîture de prothèse. Elles permettent le raccordement aux
20 | Ottobock
4R111
4R111=N
155
80
44
13
Stainless steel
150
4R116
165
2
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