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EN ISO 13408-1
6 current listing(s) — 2 EU harmonised, 4 UK designated.
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Current listings
| Edition | List | Title | Presumption from | Withdrawal / cessation | |
|---|---|---|---|---|---|
| EN ISO 13408-1:2015 | UK UK IVD (designated) | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013) | 01/01/2021 | 17/01/2026 | source |
| EN ISO 13408-1:2015 | UK UK Medical Devices (designated) | Aseptic processing of health care products - Part 1: General requirements | 01/01/2021 | source | |
| EN ISO 13408-1:2024 | EU IVD Regulation | Aseptic processing of health care products – Part 1: General requirements (ISO 13408-1:2023) | source | ||
| EN ISO 13408-1:2024 | EU Medical Devices Regulation | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2023) | source | ||
| EN ISO 13408-1:2024 | UK UK IVD (designated) | Aseptic processing of health care products - Part 1: General requirements | 17/01/2026 | source | |
| EN ISO 13408-1:2024 | UK UK Medical Devices (designated) | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013) | 17/01/2026 | source |
Timeline
- 2024-10-09listed in Medical Devices Regulation
EN ISO 13408-1:2024 - 2024-10-09listed in IVD Regulation
EN ISO 13408-1:2024
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