DS/EN ISO 10993-17:2023
Current
Current
The latest, up-to-date edition.
Biological evaluation of medical devices – Part 17: Toxicological risk assessment of medical device constituents
Published date
30-11-2023
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 |
Standard
|
| ProductNote |
This standard identical is also ISO 10993-17
|
| PublisherName |
Danish Standards
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| EN ISO 10993-17:2009 | Identical |
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