CEN/TC 102
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 37474 | EN ISO 15883-1:2009/A1:2014 | Washer-disinfectors - Part 1: General requirements, terms and definitions and tests (ISO 15883-1:2006/Amd 1:2014) | Atcelts |
| 31451 | EN ISO 15883-1:2009 | Washer-disinfectors - Part 1: General requirements, terms and definitions and tests (ISO 15883-1:2006) | Atcelts |
| 24487 | EN ISO 15883-1:2006 | Washer-disinfectors - Part 1: General requirements, terms and definitions and tests (ISO 15883-1:2006) | Atcelts |
| 26692 | EN ISO 15882:2008 | Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results (ISO 15882:2008) | Izstrādē |
| 2455 | EN ISO 15882:2003 | Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results (ISO 15882:2003) | Atcelts |
| 26693 | EN ISO 14161:2009 | Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (ISO/FDIS 14161:2009) | Atcelts |
| 2451 | EN ISO 14161:2000 | Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (ISO 14161:2000) | Atcelts |
| 72114 | EN ISO 11607-2:2020/A1:2023 | Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1: Application of risk management (ISO 11607-2:2019/Amd 1:2023) | Standarts spēkā |
| 76018 | EN ISO 11607-2:2020/A11:2022 | Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019) | Izstrādē |
| 62250 | EN ISO 11607-2:2020 | Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019) | Standarts spēkā |
Displaying 181-190 of 317 results.