Registration number (WIID)Project No.TitleStatus
60165ISO 11137-1:2006/Amd 1:2013Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices — Amendment 1Atcelts
31457ISO 11607:2003Packaging for terminally sterilized medical devicesAtcelts
44955ISO 11737-2:2009Sterilization of medical devices — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization processAtcelts
66566ISO/TS 19930:2017Guidance on aspects of a risk-based approach to assuring sterility of terminally sterilized, single-use health care product that is unable to withstand processing to achieve maximally a sterility assurance level of 10-6Atcelts
62952ISO 17664:2017Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devicesAtcelts
53573ISO/TS 11135-2:2008/Cor 1:2009Sterilization of health care products — Ethylene oxide — Part 2: Guidance on the application of ISO 11135-1 — Technical Corrigendum 1Atcelts
40168ISO/TS 11139:2006Sterilization of health care products — VocabularyAtcelts
41175ISO/TS 15883-5:2005Washer-disinfectors — Part 5: Test soils and methods for demonstrating cleaning efficacyAtcelts
24811ISO 11135:1994/Cor 1:1994Medical devices — Validation and routine control of ethylene oxide sterilization — Technical Corrigendum 1Atcelts
35047ISO 18472:2006Sterilization of health care products — Biological and chemical indicators — Test equipmentAtcelts
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