
Medical devices - Information supplied by the manufacturer
出版:German Institute for Standardisation (Deutsches Institut für Normung)

专家解读视频
Defines requirements for the information for supplying by a manufacturer for different categories of medical devices as required by the relevant EU Directives. Does not define the language to be used for such information. Meant to complement the specified requirements of the EU Directives on medical devices in the context of defining means where certain requirements may be met.
DRAFT 2006 issued in Oct. 2006. (10/2006)
NF EN 1041:2008 - Identical
NEN EN 1041:2008 - Identical
SS EN 1041 Ed. 2 (2008) - Identical
UNE EN 1041:1998 - Identical
SS EN 1041 Ed. 1 (1998) - Identical
NS EN 1041 Ed. 1 (1998) - Identical
I.S. EN 1041:1998 - Identical
UNI EN 1041:2000 - Identical
NF EN 1041:1998 - Identical
NBN EN 1041:1998 - Identical
ONORM EN 1041:1998 - Identical
BS EN 1041:1998 - Identical
NEN EN 1041:1998 - Identical
SN EN 1041:1998 - Identical