Registration number (WIID)Project No.TitleStatus
37341LVS EN ISO 13408-6:2011/ A1:2013Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005/Amd 1:2013)Atcelts
9301EN 556-1:2001Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devicesAtcelts
9299EN 13824:2004Sterilization of medical devices - Aseptic processing of liquid medical devices - RequirementsAtcelts
32632LVS EN ISO 11137-2:2007 /AC:2009Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006/Cor 1:2009)Atcelts
9309EN ISO 11137-2:2012Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2012)Atcelts
9293EN 1174-2:1996Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 2: GuidanceAtcelts
41915LVS EN ISO 17664:2018Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)Atcelts
9299LVS EN 13824:2005Sterilization of medical devices - Aseptic processing of liquid medical devices - RequirementsAtcelts
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
27794LVS EN 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 14160:2011)Atcelts
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