SS-EN ISO 10993-5:2009

Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)

Standard · Swedish standard
SS-EN ISO 10993-5:2009

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  • 1 st·STANDARD SS-EN ISO 10993-1:2009
  • 1 st·STANDARD SS-EN ISO 10993-1:2009/AC:2010
  • 1 st·STANDARD SS-EN ISO 10993-2:2006
  • 1 st·STANDARD SS-EN ISO 10993-4:2009
  • 1 st·STANDARD SS-EN ISO 10993-5:2009
  • 1 st·STANDARD SS-EN ISO 10993-6:2009
  • 1 st·STANDARD SS-EN ISO 10993-7:2008
  • 1 st·STANDARD SS-EN ISO 10993-7:2008/AC:2009
  • 1 st·STANDARD SS-EN ISO 10993-9:2009
  • 1 st·STANDARD SS-EN ISO 10993-10:2010
  • 1 st·STANDARD SS-EN ISO 10993-11:2009
  • 1 st·STANDARD SS-EN ISO 10993-12:2012
  • 1 st·STANDARD SS-EN ISO 10993-13:2010
  • 1 st·STANDARD SS-EN ISO 10993-14:2009
  • 1 st·STANDARD SS-EN ISO 10993-15:2009
  • 1 st·STANDARD SS-EN ISO 10993-16:2010
  • 1 st·STANDARD SS-EN ISO 10993-17:2009
  • 1 st·STANDARD SS-EN ISO 10993-18:2009
  • 1 st·STANDARD ISO/TS 10993-19:2006
  • 1 st·STANDARD ISO/TS 10993-20:2006
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This part of ISO 10993 describes test methods to assess the in vitro cytotoxicity of medical devices.

These methods specify the incubation of cultured cells in contact with a device and/or extracts of a device either directly or through diffusion.

These methods are designed to determine the biological response of mammalian cells in vitro using appropriate biological parameters.

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