DS/EN ISO 10993-17:2023/A1:2025
Current
Current
The latest, up-to-date edition.
Biological evaluation of medical devices – Part 17: Toxicological risk assessment of medical device constituents – Amendment 1 (ISO 10993-17:2023/Amd 1:2025)
Amendment of
Published date
05-01-2026
Publisher
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This document specifies the process and requirements for the toxicological risk assessment of medical device constituents.
| Committee |
DS/S-258
|
| DocumentType |
Amendment
|
| PublisherName |
Danish Standards
|
| Status |
Current
|
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