Registration number (WIID)Project No.TitleStatus
35153LVS EN ISO 13408-6:2011Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)Atcelts
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
65050LVS EN ISO 13408-6:2021Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2021)Standarts spēkā
40897LVS EN ISO 13408-7:2015Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)Standarts spēkā
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
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
65357LVS EN ISO 14160:2021Sterilization 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 14160:2020)Standarts spēkā
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
23112LVS EN ISO 14937:2002 /AC:2004Sterilization 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
24012LVS EN ISO 14937:2002 /AC:2005Sterilization 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
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