NF EN ISO 11135-1:2007现行
Sterilization Of Health Care Products - Ethylene Oxide - 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
Describes requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices.
Indice de classement: S98-101-1. (08/2007)
DIN EN ISO 11135-1 (2007-08) - Identical
ISO 11135-1 : 2007 - Identical
I.S. EN ISO 11135-1:2007 - Identical
NS EN ISO 11135-1 Ed. 1 (2007) - Identical
UNE EN ISO 11135-1:2007 - Identical
SS EN ISO 11135-1 Ed. 1 (2007) - Identical
NEN EN ISO 11135-1:2007 - Identical
ONORM EN ISO 11135-1:2007 - Identical
ISO 11135-1:2007 - Identical
UNI EN ISO 11135-1:2008 - Identical
BS EN ISO 11135-1:2007 - Identical
NBN EN ISO 11135-1:2007 - Identical
SN EN ISO 11135-1:2007 - Identical
