SN EN ISO 11607-1:2006被替代
Packaging For Terminally Sterilized Medical Devices - Part 1: Requirements For Materials, Sterile Barrier Systems And Packaging Systems
出版：Swiss Standards
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 SN EN 868-1. (07/2006)
NS EN ISO 11607-1 Ed. 1 (2006) - Identical
NF EN ISO 11607-1:2006 - Identical
I.S. EN ISO 11607-1:2006 - Identical
UNI EN ISO 11607-1:2006 - Identical
SS EN ISO 11607-1 Ed. 1 (2006) - Identical
NEN EN ISO 11607-1:2006 - Identical
UNE EN ISO 11607-1:2007 - Identical
ONORM EN ISO 11607-1:2007 - Identical
ISO 11607-1:2006 - Identical
NS EN ISO 11607-1:2009 - Identical
NBN EN ISO 11607-1:2009 - Identical
UNE EN ISO 11607-1:2009 - Identical
NEN EN ISO 11607-1:2009 - Identical
UNI EN ISO 11607-1:2009 - Identical
NF EN ISO 11607-1:2009 - Identical
BS EN ISO 11607-1:2006 - Identical
DIN EN ISO 11607-1 (2006-07) - Identical
NBN EN ISO 11607-1:2006 - Identical
