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EN ISO 10993-17
3 current listing(s) — 1 EU harmonised, 2 UK designated.
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Current listings
| Edition | List | Title | Presumption from | Withdrawal / cessation | |
|---|---|---|---|---|---|
| EN ISO 10993-17:2009 | UK UK Medical Devices (designated) | Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) | 01/01/2021 | source | |
| EN ISO 10993-17:2023 | EU Medical Devices Regulation | Biological evaluation of medical devices – Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023) | source | ||
| EN ISO 10993-17:2023 | UK UK Medical Devices (designated) | Biological evaluation of medical devices – Part 17: Toxicological risk assessment of medical device constituents | 17/01/2026 | source |
Timeline
- 2024-03-08listed in Medical Devices Regulation
EN ISO 10993-17:2023
JSON: /api/v1/standard/en-iso-10993-17.json
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