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ISO/DIS 10993-16:2025
Biological evaluation of medical devices
Part 16: Toxicokinetic evaluation for degradation products and leachables
Part 16: Toxicokinetic evaluation for degradation products and leachables
Summary
ISO 10993-16:2017 provides principles on designing and performing toxicokinetic evaluation relevant to medical devices. Annex A describes the considerations for inclusion of toxicokinetic evaluation in the biological evaluation of medical devices.
Notes
40.00 : DIS enregistré
Technical characteristics
| Publisher | International Organization for Standardization (ISO) |
| Publication Date | 12/08/2025 |
| Edition | 4 |
| Page Count | 21 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
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16/05/2017
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, Reaffirmed
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Previous versions
16/05/2017
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, Reaffirmed
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