Registration number (WIID)Project No.TitleStatus
38073LVS EN ISO 20857:2013Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010)Standarts spēkā
38073EN ISO 20857:2013Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010)Standarts spēkā
37754EN ISO 11137-1:2006/A1:2013Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/Amd 1:2013)Atcelts
37754LVS EN ISO 11137-1:2006 /A1:2013Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/Amd 1:2013)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
37341EN ISO 13408-6:2011/A1:2013Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005/Amd 1:2013)Atcelts
37321EN ISO 13408-1:2011/A1:2013Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013)Atcelts
37321LVS EN ISO 13408-1:2011 /A1:2013Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008/Amd 1:2013)Atcelts
36593EN ISO 11135:2014Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014)Standarts spēkā
36593LVS EN ISO 11135:2014Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014)Standarts spēkā
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