SN EN ISO 11737-2:2010现行
Sterilization Of Medical Devices - Microbiological Methods - Part 2: Tests Of Sterility Performed In The Definition, Validation And Maintenance Of A Sterilization Process
出版：Swiss Standards
专家解读视频
Establishes the general requirements for tests on medical devices that have been exposed to a treatment with the sterilizing agent that is a fraction of the specified sterilization process. These tests are intended to be carried out when validating a sterilization process. Does not apply to sterility testing for routine release of product that has been subjected to a sterilization process, nor to performance of a pharmacopoeial sterility test.
UNE EN ISO 11737-2:2010 - Identical
ONORM EN ISO 11737-2:2010 - Identical
SS EN ISO 11737-2 Ed. 2 (2009) - Identical
I.S. EN ISO 11737-2:2009 - Identical
NEN EN ISO 11737-2:2009 - Identical
BS EN ISO 11737-2:2009 - Identical
NF EN ISO 11737-2:2010 - Identical
NBN EN ISO 11737-2:2010 - Identical
NS EN ISO 11737-2:2009 - Identical
UNI EN ISO 11737-2:2010 - Identical
DIN EN ISO 11737-2 (2010-04) - Identical
