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    • Other standards related to sterilization and disinfection
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    ISO/IEC 29138-1:2018

    Information technology -- User interface accessibility -- Part 1: User accessibility needs

    International Organization for Standardization

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    ASTM E 2720 : 2016

    Standard Practice for Evaluation of Effectiveness of Decontamination Procedures for Air-Permeable Materials when Challenged with Biological Aerosols Containing Human Pathogenic Viruses

    American Society for Testing and Materials

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    ASTM E 2721 : 2016 : REDLINE

    Standard Practice for Evaluation of Effectiveness of Decontamination Procedures for Surfaces When Challenged with Droplets Containing Human Pathogenic Viruses

    American Society for Testing and Materials

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    ASTM E 2721 : 2016

    Standard Practice for Evaluation of Effectiveness of Decontamination Procedures for Surfaces When Challenged with Droplets Containing Human Pathogenic Viruses

    American Society for Testing and Materials

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    ASTM E 2720 : 2016 : REDLINE

    Standard Practice for Evaluation of Effectiveness of Decontamination Procedures for Air-Permeable Materials when Challenged with Biological Aerosols Containing Human Pathogenic Viruses

    American Society for Testing and Materials

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    ASTM E 2314 : 2003 : R2014

    Standard Test Method for Determination of Effectiveness of Cleaning Processes for Reusable Medical Instruments Using a Microbiologic Method (Simulated Use Test)

    American Society for Testing and Materials

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    ASTM D 4196 : 2005 : R2011

    Standard Test Method for Confirming the Sterility of Membrane Filters

    American Society for Testing and Materials

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    SS-EN 1276:2019

    Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in food, industrial, domestic and institutional areas - Test method and requirements (phase 2, step 1)

    Standardiserings-Kommissionen I Sverige

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    SS-ISO 11156:2011

    Packaging - Accessible design - General requirements (ISO 11156:2011, IDT)

    Standardiserings-Kommissionen I Sverige

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    SS-EN ISO 11137-1:2015

    Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)

    Standardiserings-Kommissionen I Sverige

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