ISO 10993-16:2010 Historical

1672748

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

standard by International Organization for Standardization , 02/15/2010

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Full Description

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.

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Document History

  1. ISO 10993-16:2017


    Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

    • Most Recent

  2. ISO 10993-16:2010

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    Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

    • Historical Version

  3. ISO 10993-16:1997


    Biological evaluation of medical devices -- Part 16: Toxicokinetic study design for degradation products and leachables

    • Historical Version

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Product Details

Published:

02/15/2010

File Size:

1 file

Same As:

BS EN ISO 10993-16:2010, DIN EN ISO 10993-16, AAMI/ISO 10993-16:2010/(R)2014

Note:

This product is restricted and cannot be purchased in the following countries Ukraine, Russia, Belarus