
Information Supplied By The Manufacturer Of Medical Devices
出版:Standardiserings-Kommissionen I Sverige

专家解读视频
Defines requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical devices and Council Directive 93/42/EEC concerning medical devices.
NBN EN 1041:1998 - Identical
ONORM EN 1041:1998 - Identical
UNI EN 1041:2000 - Identical
NS EN 1041 Ed. 1 (1998) - Identical
UNE EN 1041:1998 - Identical
UNE EN 1041:2009 - Identical
NS EN 1041 Ed. 2 (2008) - Identical
SN EN 1041:2008 - Identical
ONORM EN 1041:2008 - Identical
DIN EN 1041 (2008-11) - Identical
NEN EN 1041:2008 - Identical
NF EN 1041:2008 - Identical
BS EN 1041:2008 - Identical
I.S. EN 1041:2008 - Identical
SN EN 1041:1998 - Identical
DIN EN 1041 (1998-04) - Identical