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About This Item

 

Full Description

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 the ISO 10993 series. Includes extraction procedures and soluble polymer procedures.
 

Document History

  1. AAMI/ISO 10993-12:2012

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    Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials

    • Most Recent
  2. AAMI/ISO 10993-12:2007


    Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials

    • Historical Version
  3. AAMI/ISO 10993-12:2002


    Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials

    • Historical Version