
Packaging For Terminally Sterilized Medical Devices - Part 1: Requirements For Materials, Sterile Barrier Systems And Packaging Systems
出版:Italian Standards

专家解读视频
Describes 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 UNI EN 868-1. (07/2006) 2006 version remains active until 22 March 2010. (09/2009)
NS EN ISO 11607-1 Ed. 1 (2006) - Identical
UNE EN ISO 11607-1:2007 - Identical
SS EN ISO 11607-1 Ed. 1 (2006) - Identical
ONORM EN ISO 11607-1:2007 - Identical
SS EN ISO 11607-1 Ed. 2 (2009) - Identical
SN EN ISO 11607-1:2009 - Identical
ONORM EN ISO 11607-1:2009 - Identical
BS EN ISO 11607-1:2009 - Identical
NS EN ISO 11607-1:2009 - Identical
NBN EN ISO 11607-1:2009 - Identical
UNE EN ISO 11607-1:2009 - Identical
DIN EN ISO 11607-1 (2009-09) - Identical
NF EN ISO 11607-1:2009 - Identical
I.S. EN ISO 11607-1:2009 - Identical
NEN EN ISO 11607-1:2009 - Identical
SN EN ISO 11607-1:2006 - Identical
NBN EN ISO 11607-1:2006 - Identical