
STERILIZATION OF MEDICAL DEVICES - MICROBIOLOGICAL METHODS - PART 2: TESTS OF STERILITY PERFORMED IN THE DEFINITION, VALIDATION AND MAINTENANCE OF A STERILIZATION PROCESS
出版:International Organization for Standardization

专家解读视频
This part of ISO 11737 Describes the general criteria for tests of sterility on medical devices that have been exposed to a treatment with the sterilizing agent reduced relative to that anticipated to be used in routine sterilization processing.
DS EN ISO 11737-2 : 2009 - Identical
AAMI ISO 11737-2 : 2009 - Identical
AAMI ISO 11737-2 : 2009 : R2014 - Identical
AAMI ISO 11737-2 : 2009 - Identical
PN EN ISO 11737-2 : DEC 2010 - Identical
GOST ISO 11737-2 : 2011 - Identical
GOST R ISO 11737-2 : 2003 - Identical
UNI EN ISO 11737-2 : 2010 - Identical
DIN EN ISO 11737-2 E : 2010 - Identical
AAMI ISO 11737-2 : 2009 - Identical
NS EN ISO 11737-2 : 2009 - Identical
UNE EN ISO 11737-2 : 2010 - Identical
NBN EN ISO 11737-2 : 2010 - Identical
BS EN ISO 11737-2 : 2009 - Identical
DIN EN ISO 11737-2 : 2010 - Identical
SN EN ISO 11737-2 : 2010 - Identical
EN ISO 11737-2 : 2009 - Identical
NF EN ISO 11737-2 : 2010 - Identical
PN EN ISO 11737-2 : DEC 2010 - Identical
GOST ISO 11737-2 : 2011 - Identical
I.S. EN ISO 11737-2:2009 - Identical
NEN EN ISO 11737-2 : 2009 - Identical
DS EN ISO 11737-2 : 2009 - Identical