CEN/TC 102
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 65298 | 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 Amd 1:2014) | Atcelts |
| 62249 | EN ISO 11607-1:2020 | Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2019) | Standarts spēkā |
| 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 |
| 72113 | EN ISO 11607-1:2020/A1:2023 | Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems - Amendment 1: Application of risk management (ISO 11607-1:2019/Amd 1:2023) | Standarts spēkā |
| 23100 | EN ISO 11607-2:2006 | Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006) | Atcelts |
| 37407 | EN ISO 11607-2:2006/A1:2014 | Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006/Amd 1:2014) | Atcelts |
| 65299 | 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, including Amd 1:2014) | Atcelts |
| 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 |
| 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 |
| 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 |
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