ISO 25424 : 2009(R2015)已作廢
STERILIZATION OF MEDICAL DEVICES - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES
出版：International Organization for Standardization
專家解讀視頻
Describes requirements for the development, validation and routine control of a Low Temperature Steam and Formaldehyde (LTSF) sterilization process for medical devices.
DS EN ISO 25424 : 2011 - Identical
SN EN ISO 25424 : 2011 - Identical
NF EN ISO 25424 : 2011 - Identical
BS EN ISO 25424 : 2011 - Identical
NBN EN ISO 25424 : 2011 - Identical
NEN ISO 25424 : 2009 - Identical
DIN EN ISO 25424 : 2011 - Identical
UNE EN ISO 25424 : 2011 - Identical
NS EN ISO 25424 : 2011 - Identical
UNI EN ISO 25424 : 2011 - Identical
NEN EN ISO 25424 : 2011 - Identical
GOST R ISO 25424 : 2013 - Identical
DIN EN ISO 25424 E : 2011 - Identical
PN EN ISO 25424 : 2013 - Identical
I.S. EN ISO 25424:2011 - Identical
