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    • Biological evaluation of medical devices
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    EN ISO 10993-13 : 2010

    BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 13: IDENTIFICATION AND QUANTIFICATION OF DEGRADATION PRODUCTS FROM POLYMERIC MEDICAL DEVICES (ISO 10993-13:2010)

    Comite Europeen de Normalisation

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    SS-EN ISO 10993-6:2017

    Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)

    Standardiserings-Kommissionen I Sverige

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    SS-EN ISO 10993-7:2008

    Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)

    Standardiserings-Kommissionen I Sverige

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    NEN-EN-ISO 10993-7 : 2008

    Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals

    Netherlands Standards

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    SS-EN ISO 10993-17:2009

    Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

    Standardiserings-Kommissionen I Sverige

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    SS-EN ISO 10993-5:2009

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

    Standardiserings-Kommissionen I Sverige

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    PN-EN ISO 10993-7: 2009

    Biological evaluation of medical devices - Part 7: Residues after sterilization with ethylene oxide

    Polish Committee for Standardization

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    SS-EN ISO 10993-9:2009

    Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)

    Standardiserings-Kommissionen I Sverige

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    SS-EN ISO 10993-2 : 2006

    Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006)

    Standardiserings-Kommissionen I Sverige

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    SN EN ISO 10993-7 : 2008

    Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)

    Swiss Standards