
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:Norwegian Standards (Norges Standardiseringsforbund)

专家解读视频
Describes requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices.
Supersedes NS EN 550. (09/2007)
UNI EN ISO 11135-1:2008 - 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
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