Registration number (WIID)Project No.TitleStatus
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
28190EN ISO 11137-2:2007Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006, corrected version 2006-08-01)Atcelts
37321EN ISO 13408-1:2011/A1:2013Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013)Atcelts
27305EN ISO 11737-1:2006/AC:2009Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006/Cor 1:2007)Atcelts
32632EN ISO 11137-2:2007/AC:2009Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006/Cor 1:2009)Atcelts
60763EN ISO 13408-1:2015Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)Atcelts
27633EN 556-1:2001/AC:2006Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devicesAtcelts
9300LVS EN 556:1994 +A1:1998Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile"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
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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