Registration number (WIID)Project No.TitleStatus
23100LVS EN ISO 11607-2:2006Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processesAtcelts
37407LVS EN ISO 11607-2:2006/A1:2014Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006/Amd 1:2014)Atcelts
65299LVS EN ISO 11607-2:2017Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)Atcelts
62250LVS EN ISO 11607-2:2020Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)Standarts spēkā
76018LVS EN 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)Standarts spēkā
72114LVS EN ISO 11607-2:2020/A1:2023Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1: Application of risk management (ISO 11607-2:2019/Amd 1:2023)Standarts spēkā
2451LVS EN ISO 14161:2002Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of resultsAtcelts
26693LVS EN ISO 14161:2010Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (ISO 14161:2009)Atcelts
2455LVS EN ISO 15882:2003Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of resultsAtcelts
26692LVS EN ISO 15882:2008Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results (ISO 15882:2008)Standarts spēkā
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