ISO 10993-16:2010
Withdrawn
View Superseded by
Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables
Hardcopy , PDF
French, English
02-09-2010
04-09-2025
ISO 10993-16:2010 gives principles on how toxicokinetic studies relevant to medical devices should be designed and performed. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.
| Committee |
ISO/TC 194
|
| DocumentType |
Standard
|
| Pages |
13
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| BS EN ISO 10993-16:2010 | Equivalent |
| DIN EN ISO 10993-16:2010-06 | Equivalent |
| I.S. EN ISO 10993-16:2010 | Equivalent |
| BS EN ISO 10993-16:2010 | Identical |
| UNE-EN ISO 10993-16:2010 | Identical |
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