Registration number (WIID)Project No.TitleStatus
59368ISO 11607-2:2006/Amd 1:2014Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1Atcelts
33832ISO 11137:1995/Amd 1:2001Sterilization of health care products — Requirements for validation and routine control — Radiation sterilization — Amendment 1: Selection of items for dose settingAtcelts
33952ISO 11137-1:2006Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devicesAtcelts
27036ISO/TR 15844:1998Sterilization of health care products — Radiation sterilization — Selection of sterilization dose for a single production batchAtcelts
38713ISO 11607-2:2006Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processesAtcelts
37842ISO 13408-1:2008Aseptic processing of health care products — Part 1: General requirementsAtcelts
21926ISO/TR 13409:1996Sterilization of health care products — Radiation sterilization — Substantiation of 25 kGy as a sterilization dose for small or infrequent production batchesAtcelts
23267ISO 11737-2:1998Sterilization of medical devices — Microbiological methods — Part 2: Tests of sterility performed in the validation of a sterilization processAtcelts
43188ISO/TS 17665-2:2009Sterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1Atcelts
20530ISO 11138-2:1994Sterilization of health care products — Biological indicators — Part 2: Biological indicators for ethylene oxide sterilizationAtcelts
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