Registration number (WIID)Project No.TitleStatus
9283EN 550:1994Sterilization of medical devices - Validation and routine control of ethylene oxide sterilizationAtcelts
9297EN ISO 14937:2000Sterilization 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
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
9302EN 552:1994/A1:1999Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
9307EN ISO 11737-2:2000Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process (ISO 11737-2:1998)Atcelts
32635CEN ISO/TS 11135-2:2008/AC:2009Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008/Cor 1:2009)Atcelts
39251EN 556-2:2015Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE'' - Part 2: Requirements for aseptically processed medical devicesAtcelts
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
37754EN ISO 11137-1:2006/A1:2013Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/Amd.1:2012)Atcelts
9289LVS EN 556:1994Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile"Atcelts
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