
Sterilization Of Medical Devices - Requirements For Medical Devices To Be Designated "sterile" - Part 2: Requirements For Aseptically Processed Medical Devices
出版:Nederlands Normalisatie Instituut

专家解读视频
Describes the requirements for an aseptically processed medical device to be designated 'STERILE'.
ONORM EN 556-2:2004 - Identical
SS EN 556-2 Ed. 1 (2004) - Identical
UNE EN 556-2:2004 - Identical
NS EN 556-2 Ed. 1 (2004) - Identical
UNI EN 556-2:2005 - Identical
I.S. EN 556-2:2004 - Identical
NF EN 556-2:2004 - Identical
NBN EN 556-2:2004 - Identical
DIN EN 556-2 (2004-03) - Identical
BS EN 556-2:2003 - Identical
SN EN 556-2:2004 - Identical
NBN EN 556-2:2015 - Identical
SN EN 556-2:2015 - Identical
SS EN 556-2 Ed. 2 (2015) - Identical
ONORM EN 556-2:2015 - Identical
EN 556-2:2015 - Identical
NF EN 556-2:2015 - Identical
UNE EN 556-2:2016 - Identical
NS EN 556-2:2015 - Identical