
Sterilization Of Health Care Products - Radiation - Part 1: Requirements For Development, Validation And Routine Control Of A Sterilization Process For Medical Devices (Iso 11137-1:2006, Including Amd 1:2013)
出版:Standardiserings-Kommissionen I Sverige

专家解读视频
Defines requirements for the development, validation and routine control of a radiation sterilization process for medical devices.
Supersedes SS EN 552 (07/2006)
BS EN ISO 11137-1:2006+A1:2013 - Identical
UNI EN ISO 11137-1:2013 - Identical
DIN EN ISO 11137-1 (2013-12) - Identical
ONORM EN ISO 11137-1:2013 - Identical
I.S. EN ISO 11137-1:2015 - Identical
NEN EN ISO 11137-1:2015 - Identical
EN ISO 11137-1:2015 - Identical
NBN EN ISO 11137-1:2006 - Identical
SN EN ISO 11137-1:2006 - Identical
UNE EN ISO 11137-1:2007 - Identical
NF EN ISO 11137-1:2006 - Identical
BS EN ISO 11137-1:2015 - Identical
SN EN ISO 11137-1:2015 - Identical
ONORM EN ISO 11137-1:2015 - Identical
NF EN ISO 11137-1:2016 - Identical
UNI EN ISO 11137-1:2015 - Identical
UNE EN ISO 11137-1:2015 - Identical