Registration number (WIID)Project No.TitleStatus
9283EN 550:1994Sterilization of medical devices - Validation and routine control of ethylene oxide sterilizationAtcelts
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
27794EN ISO 14160:2011Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO/DIS 14160:2009)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
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
39251LVS EN 556-2:2016Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devicesAtcelts
27133LVS CEN 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
35154EN ISO 13408-1:2011Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008)Atcelts
9296LVS EN ISO 14160:1998Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilantsAtcelts
9301LVS EN 556-1:2002Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesAtcelts
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