
Information Supplied By The Manufacturer Of Medical Devices
出版:Norwegian Standards (Norges Standardiseringsforbund)

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.
I.S. EN 1041:2008 - Identical
BS EN 1041:2008 - Identical
NF EN 1041:2008 - Identical
NEN EN 1041:2008 - Identical
SS EN 1041 Ed. 2 (2008) - Identical
DIN EN 1041 (2008-11) - Identical
ONORM EN 1041:2008 - Identical
SN EN 1041:2008 - Identical
UNE EN 1041:2009 - Identical
UNE EN 1041:1998 - Identical
UNI EN 1041:2000 - Identical
ONORM EN 1041:2013 - Identical