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
38712ISO 11607-1:2006Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systemsAtcelts
19542ISO 11607:1997Packaging for terminally sterilized medical devicesAtcelts
33958ISO 11138-3:2006Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processesAtcelts
43187ISO 17665-1:2006Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devicesAtcelts
38546ISO 14937:2000/Cor 1:2003Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices — Technical Corrigendum 1Atcelts
27035ISO/TS 15843:2000Sterilization of health care products — Radiation sterilization — Product families and sampling plans for verification dose experiments and sterilization dose audits, and frequency of sterilization dose auditsAtcelts
24811ISO 11135:1994/Cor 1:1994Medical devices — Validation and routine control of ethylene oxide sterilization — Technical Corrigendum 1Atcelts
30058ISO 13408-2:2003Aseptic processing of health care products — Part 2: FiltrationAtcelts
43186ISO/TS 11135-2:2008Sterilization of health care products — Ethylene oxide — Part 2: Guidance on the application of ISO 11135-1Atcelts
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