Registration number (WIID)Project No.TitleStatus
31456ISO 17664:2004Sterilization of medical devices — Information to be provided by the manufacturer for the processing of resterilizable medical devicesAtcelts
43185ISO 11135-1:2007Sterilization of health care products — Ethylene oxide — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devicesAtcelts
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
51238ISO 11137-2:2012Sterilization of health care products — Radiation — Part 2: Establishing the sterilization doseAtcelts
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
59368ISO 11607-2:2006/Amd 1:2014Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes — Amendment 1Atcelts
41077ISO 15883-2:2006Washer-disinfectors — Part 2: Requirements and tests for washer-disinfectors employing thermal disinfection for surgical instruments, anaesthetic equipment, bowls, dishes, receivers, utensils, glassware, etc.Atcelts
41076ISO 15883-1:2006Washer-disinfectors — Part 1: General requirements, terms and definitions and testsAtcelts
62952ISO 17664:2017Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devicesAtcelts
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