Registration number (WIID)Project No.TitleStatus
27633LVS EN 556-1:2002 /AC:2007Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesAtcelts
9297LVS EN ISO 14937:2002Sterilization 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 devicesAtcelts
28190LVS EN ISO 11137-2:2007Sterilization of health care products - Radiation - Part 2: Establishing the sterilization doseAtcelts
9299LVS EN 13824:2005Sterilization of medical devices - Aseptic processing of liquid medical devices - RequirementsAtcelts
9283EN 550:1994Sterilization of medical devices - Validation and routine control of ethylene oxide sterilizationAtcelts
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
9306EN 552:1994/A2:2000Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
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
39251LVS EN 556-2:2016Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devicesAtcelts
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
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