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About This Item

 

Full Description

BS EN ISO 10993-5:2009 describes test methods to assess the in vitro cytotoxicity of medical devices.

BS EN ISO 10993-5:2009 specify the incubation of cultured cells in contact with a device and/or extracts of a device either directly or through diffusion.

BS EN ISO 10993-5:2009 are designed to determine the biological response of mammalian cells in vitro using appropriate biological parameters.



Cross References:
ISO 10993-1
ISO 10993-12
93/42/EEC
90/385/EEC


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

Document History

  1. BS EN ISO 10993-5:2009

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    Biological evaluation of medical devices

    • Most Recent
  2. BS 07/30160957 DC


    EN ISO 10993-5. Biological evaluation of medical devices. Part 5. Tests for in vitro cytotoxicity

    • Historical Version
  3. BS EN ISO 10993-5:1999


    Biological evaluation of medical devices. Tests for in vitro cytotoxicity

    • Historical Version