CEN/TC 204
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 27633 | LVS EN 556-1:2002 /AC:2007 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | Atcelts |
| 76163 | LVS EN 556-1:2024 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices | Standarts spēkā |
| 9289 | LVS EN 556:1994 | Sterilization of medical devices - Requirements for medical devices to be labelled "Sterile" | Atcelts |
| 9300 | LVS EN 556:1994 +A1:1998 | Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile" | Atcelts |
| 21434 | LVS EN 556-2:2004 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices | Atcelts |
| 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 |
| 76162 | LVS EN 556-2:2024 | Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices | |
| 9303 | LVS EN ISO 11135-1:2007 | Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices | Atcelts |
| 36593 | LVS EN ISO 11135:2014 | Sterilization 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 |
| 62262 | LVS EN ISO 11135:2014/A1:2020 | Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/Amd 1:2018) | Standarts spēkā |
Displaying 101-110 of 173 results.