SN EN 1041:2008现行
Information Supplied By The Manufacturer Of Medical Devices
出版：Swiss Standards
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.
2008 Edition Re-Issued in October 2013 & incorporates AMD 1 2013. (11/2013)
UNI EN 1041:2000 - Identical
UNE EN 1041:1998 - Identical
NBN EN 1041:2008 - Identical
DIN EN 1041 (2013-12) - Identical
ONORM EN 1041:2013 - Identical
BS EN 1041:2008+A1:2013 - Identical
UNE EN 1041:2009 - Identical
NS EN 1041 Ed. 2 (2008) - Identical
ONORM EN 1041:2008 - Identical
DIN EN 1041 (2008-11) - Identical
SS EN 1041 Ed. 2 (2008) - Identical
NEN EN 1041:2008 - Identical
NF EN 1041:2008 - Identical
BS EN 1041:2008 - Identical
I.S. EN 1041:2008 - Identical
