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About This Item

 

Full Description

Intended to assess haemolytic effects in vitro of leachable endogenous or extraneous substances present in or on a medical device as a result of direct contact between device material and rabbit blood. The method involves quantification of haemolysis by spectrophotometric measurement of plasma haemoglobin.

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Document History

  1. BS EN ISO 10993-4:2017


    Biological evaluation of medical devices-Selection of tests for interactions with blood

    • Most Recent
  2. BS EN ISO 10993-4:2009


    Biological evaluation of medical devices-Selection of tests for interactions with blood

    • Historical Version
  3. BS EN ISO 10993-4:2002


    Biological evaluation of medical devices-Selection of tests for interactions with blood

    • Historical Version
  4. BS EN 30993-4:1994


    Biological evaluation of medical devices-Selection of tests for interactions with blood

    • Historical Version
  5. BS 5736-11:1990

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    Evaluation of medical devices for biological hazards-Method of test for haemolysis

    • Historical Version