
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/Amd 1:2013)
出版:Swiss Standards

专家解读视频
Specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.
Supersedes SN EN 552. (07/2006)
EN ISO 11137-1:2015 - Identical
UNE EN ISO 11137-1:2015 - Identical
UNI EN ISO 11137-1:2015 - Identical
NF EN ISO 11137-1:2016 - Identical
SS EN ISO 11137-1 Ed. 2 (2015) - Identical
ONORM EN ISO 11137-1:2015 - Identical
NEN EN ISO 11137-1:2015 - Identical
BS EN ISO 11137-1:2015 - Identical
I.S. EN ISO 11137-1:2006 - Identical
NF EN ISO 11137-1:2006 - Identical
UNI EN ISO 11137-1:2006 - Identical
NS EN ISO 11137-1 Ed. 1 (2006) - Identical
UNE EN ISO 11137-1:2007 - Identical
SS EN ISO 11137-1 Ed. 1 (2006) - Identical
ISO 11137-1:2006 - Identical
NEN EN ISO 11137-1:2006 - Identical
ONORM EN ISO 11137-1:2006 - Identical
UNI EN ISO 11137-1:2013 - Identical
BS EN ISO 11137-1:2006+A1:2013 - Identical
ONORM EN ISO 11137-1:2013 - Identical
DIN EN ISO 11137-1 (2013-12) - Identical
BS EN ISO 11137-1:2006 - Identical
DIN EN ISO 11137-1 (2006-07) - Identical
NBN EN ISO 11137-1:2006 - Identical