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About This Item

 

Full Description

This document specifies requirements and gives guidance on the procedures in the preparation of samples and the selection of reference materials for medical device testing primarily in biological test systems primarily in accordance with one or more parts of the ISO 10993 series.

All current amendments available at time of purchase are included with the purchase of this document.

 

Document History

  1. BS EN ISO 10993-12:2021

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    Biological evaluation of medical devices-Sample preparation and reference materials

    • Most Recent
  2. BS EN ISO 10993-12:2012


    Biological evaluation of medical devices-Sample preparation and reference materials

    • Historical Version
  3. BS EN ISO 10993-12:2009


    Biological evaluation of medical devices-Sample preparation and reference materials

    • Historical Version
  4. BS EN ISO 10993-12:2007


    Biological evaluation of medical devices-Sample preparation and reference materials

    • Historical Version
  5. BS 06/30145887 DC


    EN ISO 10993-12. Biological evaluation of medical devices. Part 12. Sample preparation and reference materials

    • Historical Version
  6. BS EN ISO 10993-12:2004


    Biological evaluation of medical devices-Sample preparation and reference materials

    • Historical Version
  7. BS EN ISO 10993-12:1997


    Biological evaluation of medical devices-Sample preparation and reference materials

    • Historical Version