
Sterilization Of Health Care Products - General Requirements For Characterization Of A Sterilizing Agent And The Development, Validation And Routine Control Of A Sterilization Process For Medical Devices
出版:Standardiserings-Kommissionen I Sverige

专家解读视频
Describes the general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a sterilization process for medical devices.
NF EN ISO 14937:2009 - Identical
UNI EN ISO 14937:2009 - Identical
NEN EN ISO 14937:2009 - Identical
NS EN ISO 14937:2009 - Identical
I.S. EN ISO 14937:2009 - Identical
BS EN ISO 14937:2009 - Identical
DIN EN ISO 14937 (2010-03) - Identical
ONORM EN ISO 14937:2010 - Identical
NBN EN ISO 14937:2009 - Identical
SN EN ISO 14937:2010 - Identical
UNE EN ISO 14937:2010 - Identical
ONORM EN ISO 14937:2005 - Identical
SN EN ISO 14937:2001 - Identical
UNE EN ISO 14937:2001 - Identical
NS EN ISO 14937 Ed. 1 (2001) - Identical
NBN EN ISO 14937:2001 - Identical