Registration number (WIID)Project No.TitleStatus
60763EN ISO 13408-1:2015Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)Atcelts
9283EN 550:1994Sterilization of medical devices - Validation and routine control of ethylene oxide sterilizationAtcelts
9302LVS EN 552:1994/A1:1999Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
27133CEN ISO/TS 11135-2:2008Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008)Atcelts
23112EN ISO 14937:2000/AC: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 (ISO 14937:2000)Atcelts
9298EN ISO 17664:2004Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004)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
41915EN ISO 17664:2017Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)Atcelts
35154EN ISO 13408-1:2011Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008)Atcelts
24012EN ISO 14937:2000/AC:2005Sterilization 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 (ISO 14937:2000)Atcelts
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