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
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
72106ISO 11137-1:2006/Amd 2:2018Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices — Amendment 2: Revision to 4.3.4 and 11.2Atcelts
21775ISO 11140-2:1998Sterilization of health care products — Chemical indicators — Part 2: Test equipment and methodsAtcelts
41175ISO/TS 15883-5:2005Washer-disinfectors — Part 5: Test soils and methods for demonstrating cleaning efficacyAtcelts
31456ISO 17664:2004Sterilization of medical devices — Information to be provided by the manufacturer for the processing of resterilizable medical devicesAtcelts
51238ISO 11137-2:2012Sterilization of health care products — Radiation — Part 2: Establishing the sterilization doseAtcelts
62952ISO 17664:2017Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devicesAtcelts
19154ISO 11135:1994Medical devices — Validation and routine control of ethylene oxide sterilizationAtcelts
19159ISO 11140-1:1995Sterilization of health care products — Chemical indicators — Part 1: General requirementsAtcelts
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