Registration number (WIID)Project No.TitleStatus
26692EN ISO 15882:2008Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results (ISO/FDIS 15882:2008)Izstrādē
2455EN ISO 15882:2003Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results (ISO 15882:2003)Atcelts
26693EN ISO 14161:2009Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (ISO/DIS 14161:2008)Atcelts
2451EN ISO 14161:2000Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (ISO 14161:2000)Atcelts
72114EN ISO 11607-2:2020/A1:2023Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1 (ISO 11607-2:2019/DAM 1:2022)Standarts spēkā
76018EN ISO 11607-2:2020/A11:2022Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)Izstrādē
62250EN ISO 11607-2:2020Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO/DIS 11607-2)Standarts spēkā
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
37407EN ISO 11607-2:2006/A1:2014Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1 (ISO 11607-2:2006/DAM 1:2013)Atcelts
23100EN ISO 11607-2:2006Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)Atcelts
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