11.100.20 : Biological evaluation of medical devices

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  • ISO 10993-1:2018

    Biological evaluation of medical devices
    Part 1: Evaluation and testing within a risk management process
    8/17/2018 - Paper - French -
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    €199.00

  • ISO 10993-11:2017

    Biological evaluation of medical devices
    Part 11: Tests for systemic toxicity
    9/14/2017 - Paper - French -
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    €174.00

  • ISO/TR 10993-22:2017

    Biological evaluation of medical devices
    Part 22: Guidance on nanomaterials
    7/14/2017 - Paper - French -
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    €223.00

  • ISO 10993-16:2017 (R2022)

    Biological evaluation of medical devices
    Part 16: Toxicokinetic study design for degradation products and leachables
    5/16/2017 - Paper - French -
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    €110.00

  • ISO 10993-4:2017 (R2023)

    Biological evaluation of medical devices
    Part 4: Selection of tests for interactions with blood
    4/12/2017 - Paper - French -
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    €223.00

  • ISO 10993-6:2016

    Biological evaluation of medical devices
    Part 6: Tests for local effects after implantation
    11/28/2016 - Paper - French -
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    €174.00

  • ISO 10993-3:2014 (R2023)

    Biological evaluation of medical devices
    Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
    9/24/2014 - Paper - French -
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    €174.00

  • ISO 10993-13:2010 (R2019)

    Biological evaluation of medical devices
    Part 13: Identification and quantification of degradation products from polymeric medical devices
    6/4/2010 - Paper - French -
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    €110.00

  • ISO 10993-7:2008/Cor 1:2009

    Biological evaluation of medical devices
    Part 7: Ethylene oxide sterilization residuals
    11/12/2009 - Paper - French -
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    €0.00

  • ISO 10993-5:2009 (R2017)

    Biological evaluation of medical devices
    Part 5: Tests for in vitro cytotoxicity
    5/20/2009 - Paper - French -
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    €174.00

  • ISO 10993-7:2008 (R2016)

    Biological evaluation of medical devices
    Part 7: Ethylene oxide sterilization residuals
    10/13/2008 - Paper - French -
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    €248.00

  • ISO 22442-3:2007 (R2022)

    Medical devices utilizing animal tissues and their derivatives
    Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents
    11/27/2007 - Paper - French -
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    €148.00

  • ISO 10993-14:2001 (R2019)

    Biological evaluation of medical devices
    Part 14: Identification and quantification of degradation products from ceramics
    11/22/2001 - Paper - French -
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    €72.00

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