ISO 11135-1:2007被替代
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：International Organization for Standardization
专家解读视频
Specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices.
DS EN ISO 11135-1:2007 - Identical
KS P ISO 11135-1:2014 - Identical
SN EN ISO 11135-1:2007 - Identical
BS EN ISO 11135-1:2007 - Identical
DIN EN ISO 11135-1 (2007-08) - Identical
NF EN ISO 11135-1:2007 - Identical
NBN EN ISO 11135-1:2007 - Identical
I.S. EN ISO 11135-1:2007 - Identical
NS EN ISO 11135-1 Ed. 1 (2007) - Identical
PN EN ISO 11135-1:2007 - 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
AAMI ISO 11135-1:2007 - Identical
UNI EN ISO 11135-1:2008 - Identical
SAC GB 18279.1 : 2015 - Identical
AAMI ISO 11135-1 : 2007 - Identical
SANS 11135-1 : 1ED 2008(R2014) - Identical
PN EN ISO 11135-1 : 2009 - Identical
DS EN ISO 11135-1 : 2007 - Identical
NBR ISO 11135-1 : 2014 - Identical
