Registration number (WIID)Project No.TitleStatus
9289EN 556:1994Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile"Atcelts
27134CEN ISO/TS 17665-2:2009Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO/TS 17665-2:2009)Atcelts
41106CEN ISO/TS 13004:2014Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO/TS 13004:2013)Atcelts
60763EN ISO 13408-1:2015Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)Atcelts
38868EN ISO 11137-2:2013Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)Atcelts
27913EN ISO 11737-2:2009Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO/FDIS 11737-2:2009)Atcelts
9311EN ISO 11137-3:2006Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006)Atcelts
9301EN 556-1:2001Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesAtcelts
9293LVS EN 1174-2:1996Sterilization of medical devices - Estimation of the population of microorganisms on product - Part 2: GuidanceAtcelts
9299EN 13824:2004Sterilization of medical devices - Aseptic processing of liquid medical devices - RequirementsAtcelts
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