
Information Supplied by the Manufacturer of Medical Devices
出版:National Standards Authority of Ireland

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.
SS EN 1041 Ed. 2 (2008) - Identical
DIN EN 1041 (2008-11) - Identical
ONORM EN 1041:2008 - Identical
SN EN 1041:2008 - Identical
NS EN 1041 Ed. 2 (2008) - Identical
NF EN 1041:2008 - Identical
NEN EN 1041:2008 - Identical
UNI EN 1041:2000 - Identical
UNE EN 1041:2009 - Identical
NBN EN 1041:2008 - Identical
ONORM EN 1041:2013 - Identical