
Sterilization Of Medical Devices - Validation And Routine Control Of Ethylene Oxide Sterilization
出版:Standardiserings-Kommissionen I Sverige

專家解讀視頻
Specifies requirements for the development, validation, process control and monitoring of the sterilisation of medical devices using ethylene oxide. Coverage includes definitions, validation, product release from sterilisation, and process control and monitoring. Also gives detailed annexes.
UNE EN 550:1995 - Identical
NS EN 550 Ed. 1 (1994) - Identical
NF EN 550:1994 - Identical
UNI EN 550:1996 - Identical
I.S. EN 550:1994 - Identical
NBN EN 550:1995 - Identical
BS EN 550:1994 - Identical
ONORM EN 550:1994 - Identical
DIN EN 550 (1994-11) - Identical
NEN EN 550:1994 - Identical
SN EN 550:1995 - Identical