
Sterilization Of Health Care Products - Radiation - Part 1: Requirements For Development, Validation And Routine Control Of A Sterilization Process For Medical Devices
出版:Association Francaise de Normalisation

专家解读视频
Specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices.
Indice de classement: S98-103-1 PR NF EN ISO 11137-1 July 2004. (07/2004)
NEN EN ISO 11137-1:2006 - Identical
SS EN ISO 11137-1 Ed. 1 (2006) - Identical
UNE EN ISO 11137-1:2007 - Identical
NS EN ISO 11137-1 Ed. 1 (2006) - Identical
UNI EN ISO 11137-1:2006 - Identical
EN ISO 11137-1:2015 - Identical
UNE EN ISO 11137-1:2015 - Identical
UNI EN ISO 11137-1:2015 - Identical
SS EN ISO 11137-1 Ed. 2 (2015) - Identical
ONORM EN ISO 11137-1:2015 - Identical
NEN EN ISO 11137-1:2015 - Identical
ONORM EN ISO 11137-1:2013 - Identical
BS EN ISO 11137-1:2015 - Identical
SN EN ISO 11137-1:2006 - Identical
BS EN ISO 11137-1:2006 - Identical
DIN EN ISO 11137-1 (2006-07) - Identical
NBN EN ISO 11137-1:2006 - Identical
I.S. EN ISO 11137-1:2006 - Identical
ONORM EN ISO 11137-1:2006 - Identical
ISO 11137-1:2006 - Identical