UNI EN ISO 11607-2:2006被替代
Packaging For Terminally Sterilized Medical Devices - Part 2: Validation Requirements For Forming, Sealing And Assembly Processes
出版：Italian Standards
專家解讀視頻
Defines the requirements for development and validation of processes for packaging medical devices that are terminally sterilized, it includes forming, sealing, and assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems.
BS EN ISO 11607-2:2006+A1:2014 - Identical
SN EN ISO 11607-2:2006 - Identical
BS EN ISO 11607-2:2006 - Identical
DIN EN ISO 11607-2 (2006-07) - Identical
UNE EN ISO 11607-2:2007 - Identical
SS EN ISO 11607-2 Ed. 1 (2006) - Identical
NEN EN ISO 11607-2:2006 - Identical
ONORM EN ISO 11607-2:2006 - Identical
NBN EN ISO 11607-2:2006 - Identical
NF EN ISO 11607-2:2006 - Identical
I.S. EN ISO 11607-2:2006 - Identical
NS EN ISO 11607-2 Ed. 1 (2006) - Identical
ISO 11607-2:2006 - Identical
