
Packaging For Terminally Sterilized Medical Devices - Part 1: Requirements For Materials, Sterile Barrier Systems And Packaging Systems (Iso 11607-1:2006/Amd 1:2014)
出版:Norwegian Standards (Norges Standardiseringsforbund)

专家解读视频
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 NS EN 868-1. (08/2006)
NEN EN ISO 11607-1:2009 - Identical
I.S. EN ISO 11607-1:2009 - Identical
NF EN ISO 11607-1:2009 - Identical
UNI EN ISO 11607-1:2009 - Identical
DIN EN ISO 11607-1 (2009-09) - Identical
UNE EN ISO 11607-1:2009 - Identical
NBN EN ISO 11607-1:2009 - Identical
ONORM EN ISO 11607-1:2009 - Identical
SN EN ISO 11607-1:2009 - Identical
SS EN ISO 11607-1 Ed. 2 (2009) - Identical
BS EN ISO 11607-1:2009+A1:2014 - Identical
EN ISO 11607-1:2017 - Identical
NEN EN ISO 11607-1:2017 - Identical
SN EN ISO 11607-1:2006 - Identical
SS EN ISO 11607-1 Ed. 1 (2006) - Identical
ONORM EN ISO 11607-1:2007 - Identical
ONORM EN ISO 11607-1:2014 - Identical
DIN EN ISO 11607-1 (2014-11) - Identical