Registration number (WIID)Project No.TitleStatus
65299EN ISO 11607-2:2017Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006, including Amd 1:2014)Atcelts
28835EN 868-9:2009Packaging for terminally sterilized medical devices - Part 9: Uncoated nonwoven materials of polyolefines - Requirements and test methodsAtcelts
2430EN 867-2:1997Non-biological systems for use in sterilizers - Part 2: Process indicators (Class A)Atcelts
65298EN ISO 11607-1:2017Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006, including Amd 1:2014)Atcelts
37406LVS EN ISO 11607-1:2009/A1:2014Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006/Amd 1:2014)Atcelts
21838LVS EN 1422:1997 /AC:2003Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methodsAtcelts
32351LVS CEN ISO/TS 16775:2014Packaging for terminally sterilized medical devices - Guidance on the application of ISO 11607-1 and ISO 11607-2 (ISO/TS 16775:2014)Atcelts
2466LVS EN 867-3:1997/AC:1998Non-biological systems for use in sterilizers - Part 3: Specification for Class B indicators for use in the Bowie and Dick testAtcelts
31474LVS EN ISO 11140-1:2009Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2005)Atcelts
33008LVS EN 1422+A1:2009Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methodsAtcelts
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