CEN/TC 102
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 76017 | EN ISO 11607-1:2020/A11:2022 | Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2019) | Izstrādē |
| 31445 | prEN ISO 11607-2 rev | Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006) | Izstrādē |
| 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 |
| 27415 | EN 1422:2014 | Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods | Izstrādē |
| 80371 | prEN ISO 11138-6 | Sterilization of health care products - Biological indicators - Part 6: Biological indicators for vaporized hydrogen peroxide sterilization processes (ISO/DIS 11138-6:2026) | Izstrādē |
| 2444 | prEN ISO 15883-1 | Washer-disinfectors - Part 1: General requirements, definitions and tests (ISO/DIS 15883-1:2003) | Izstrādē |
| 72736 | EN ISO 11138-8:2021 | Sterilization of health care products - Biological indicators - Part 8: Method for validation of a reduced incubation time for a biological indicator (ISO 11138-8:2021) | Izstrādē |
| 65299 | LVS EN ISO 11607-2:2017 | Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006) | Atcelts |
| 65298 | LVS EN ISO 11607-1:2017 | Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006, including Amd1:2014) | Atcelts |
| 22358 | LVS EN ISO 11138-3:2006 | Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes | Atcelts |
Displaying 51-60 of 329 results.