CEN/TC 204
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
40897 | LVS EN ISO 13408-7:2015 | Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012) | Standarts spēkā |
39976 | EN ISO 11137-3:2017 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017) | Izstrādē |
39976 | LVS EN ISO 11137-3:2017 | Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017) | Standarts spēkā |
39251 | LVS EN 556-2:2016 | Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices | Standarts spēkā |
39251 | EN 556-2:2015 | Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices | Atcelts |
38868 | EN ISO 11137-2:2013 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013) | Atcelts |
38868 | LVS EN ISO 11137-2:2013 | Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013) | Atcelts |
38073 | EN ISO 20857:2013 | Sterilization 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 |
38073 | LVS EN ISO 20857:2013 | Sterilization 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 |
37754 | EN ISO 11137-1:2006/A1:2013 | Sterilization 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 |
Displaying 61-70 of 173 results.