ISO 10993-12:2012 Historical

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Biological evaluation of medical devices - Part 12: Sample preparation and reference materials

standard by International Organization for Standardization , 07/01/2012

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Full Description

ISO 10993-12:2012 specifies requirements and gives guidance on the procedures to be followed in the preparation of samples and the selection of reference materials for medical device testing in biological systems in accordance with one or more parts of ISO 10993. Specifically, ISO 10993-12:2012 addresses the following:

  • test sample selection;
  • selection of representative portions from a device;
  • test sample preparation;
  • experimental controls;
  • selection of, and requirements for, reference materials;
  • preparation of extracts.

ISO 10993-12:2012 is not applicable to live cells, but can be relevant to the material or device components of combination products containing live cells.

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Document History

  1. ISO 10993-12:2021


    Biological evaluation of medical devices - Part 12: Sample preparation and reference materials

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  2. ISO 10993-12:2012

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    Biological evaluation of medical devices - Part 12: Sample preparation and reference materials

    • Historical Version

  3. ISO 10993-12:2007


    Biological evaluation of medical devices - Part 12: Sample preparation and reference materials

    • Historical Version

  4. ISO 10993-12:2002


    Biological evaluation of medical devices - Part 12: Sample preparation and reference materials

    • Historical Version

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Product Details

Published:

07/01/2012

File Size:

1 file

Same As:

DIN EN ISO 10993-12, AAMI/ISO 10993-12:2012, BS EN ISO 10993-12:2012

Note:

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