DIN EN ISO 10993-16:2010
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010); German version EN ISO 10993-16:2010
- Standard No.
- DIN EN ISO 10993-16:2010
- Release Date
- 2010
- Published By
- German Institute for Standardization
- Status
- 2018-02
- Replace By
- DIN EN ISO 10993-16:2018
- DIN EN ISO 10993-16 E:2016
- Latest
- DIN EN ISO 10993-16:2018-02
- Scope
- This part of ISO 10993 gives principles on how toxicokinetic studies relevant to medical devices should be designed and performed.
DIN EN ISO 10993-16:2010 history
- 2018 DIN EN ISO 10993-16:2018-02 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017); German version EN ISO 10993-16:2017
- 2018 DIN EN ISO 10993-16:2018 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
- 2010 DIN EN ISO 10993-16:2010 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010); German version EN ISO 10993-16:2010
