EN ISO 10993-16:2010
Withdrawn
Withdrawn
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)
Published date
02-15-2010
Publisher
Withdrawn date
08-31-2010
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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.
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Withdrawn
|
| 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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