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About This Item

 

Full Description

This part of ISO 10993 provides general requirements for the design of tests in a simulated environment for identifying and quantifying degradation products from finished polymeric medical devices ready for clinical use.
 

Document History

  1. AAMI/ISO 10993-13:2010/(R)2019

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    Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric devices

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  2. AAMI/ISO 10993-13:1999/(R)2004


    Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric devices

    • Historical Version