Registration number (WIID)Project No.TitleStatus
9301LVS EN 556-1:2002Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesAtcelts
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
32635LVS CEN 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
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
9303LVS EN ISO 11135-1:2007Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devicesAtcelts
60763LVS EN ISO 13408-1:2015Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)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
39251EN 556-2:2015Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE'' - Part 2: Requirements for aseptically processed medical devicesAtcelts
9307LVS EN ISO 11737-2:2001Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization processAtcelts
9306EN 552:1994/A2:2000Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
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