专家解读视频
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.
NS EN 550 Ed. 1 (1994) - Identical
NEN EN 550:1994 - Identical
SN EN 550:1995 - Identical
DIN EN 550 (1994-11) - Identical
ONORM EN 550:1994 - Identical
BS EN 550:1994 - Identical
I.S. EN 550:1994 - Identical
UNI EN 550:1996 - Identical
NF EN 550:1994 - Identical
SS EN 550 Ed. 1 (1995) - Identical
UNE EN 550:1995 - Identical
