
Information Supplied By The Manufacturer Of Medical Devices
出版:Belgian Standards

专家解读视频
Describes 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.
2008 Edition Re-Issued in November 2013 & incorporates AMD 1 2013. (02/2014)
NEN EN 1041:2008 - Identical
SN EN 1041:2008 - Identical
BS EN 1041:2008+A1:2013 - Identical
UNE EN 1041:2009 - Identical
NF EN 1041:2008 - Identical
I.S. EN 1041:2008 - Identical
UNI EN 1041:2000 - Identical
DIN EN 1041 (2013-12) - Identical
ONORM EN 1041:2013 - Identical