BS EN ISO 11607-1:2009+A1:2014現行
Packaging For Terminally Sterilized Medical Devices - Part 1: Requirements For Materials, Sterile Barrier Systems And Packaging Systems
出版：British Standards Institution
專家解讀視頻
Defines the requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical devices until the point of use.
Supersedes BS EN 868-1 & 04/30101211 DC. (05/2006) 2009 Edition Re-Issued in August 2014 & incorporates AMD 1 2014. Supersedes 14/30255135 DC. (09/2014)
NBN EN ISO 11607-1:2009 - Identical
EN ISO 11607-1:2017 - Identical
ONORM EN ISO 11607-1:2018 - Identical
NEN EN ISO 11607-1:2017 - Identical
NF EN ISO 11607-1:2009 - Identical
SN EN ISO 11607-1:2009 - Identical
NEN EN ISO 11607-1:2009 - Identical
NS EN ISO 11607-1:2009 - Identical
SN EN ISO 11607-1:2018 - Identical
ONORM EN ISO 11607-1:2014 - Identical
SS EN ISO 11607-1 Ed. 3 (2018) - Identical
UNE EN ISO 11607-1:2017 - Identical
UNE EN ISO 11607-1:2009 - Identical
NS EN ISO 11607-1:2017 - Identical
