Registration number (WIID)Project No.TitleStatus
9300LVS EN 556:1994 +A1:1998Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile"Atcelts
9285LVS EN 552:2001 +A1 +A2Sterilization of medical devices - Validation and routine control of sterilization by irradiationAtcelts
9309LVS EN ISO 11137-2:2012Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2012)Atcelts
9307LVS EN ISO 11737-2:2001Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization processAtcelts
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
20669EN ISO 11737-1:2006Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006)Atcelts
9293EN 1174-2:1996Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 2: GuidanceAtcelts
9309EN ISO 11137-2:2012Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2012)Atcelts
9299EN 13824:2004Sterilization of medical devices - Aseptic processing of liquid medical devices - RequirementsAtcelts
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