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    Common aspects of electrical equipment used in medical practice

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    Medical device software - Software life cycle processes
    IEC 62304:2006 (EN-FR) forword
    Medical device software - Software life cycle processes

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    • $ 403.30 424.53 | PDF |
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    Medical devices - Guidance on the application of ISO 14971
    ISO TR 24971:2020 forword
    Medical devices - Guidance on the application of ISO 14971

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    • $ 244.19 257.05 | PDF |
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    Health software and health IT systems safety, effectiveness and security - Part 1: Principles and concepts
    ISO 81001-1:2021 forword
    Health software and health IT systems safety, effectiveness and security - Part 1: Principles and concepts

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    • $ 219.88 231.46 | PDF |
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    Guidelines for administrative, medical and nursing staff concerned with the safe use of medical electrical equipment and medical electrical systems
    IEC TR 60930:2008 forword
    Guidelines for administrative, medical and nursing staff concerned with the safe use of medical electrical equipment and medical electrical systems

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    • $ 220.99 232.62 | PDF |
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    Graphical symbols for electrical equipment in medical practice
    IEC TR 60878:2022 forword
    Graphical symbols for electrical equipment in medical practice

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    • $ 497.23 523.40 | PDF |
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    Amendment 1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
    IEC 60601-1:2005/AMD1:2012 (EN-FR) forword
    Amendment 1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

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    Medical electrical equipment - ALL PARTS
    IEC 60601-1:2023 SER (EN-FR) forword
    Medical electrical equipment - ALL PARTS

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    • $ 7,213.08 7,592.72 | PDF |
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    Medical electrical equipment - Part 1-9: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design
    IEC 60601-1-9:2007+AMD1:2013 CSV (EN-FR) forword
    Medical electrical equipment - Part 1-9: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design

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    • $ 392.26 412.90 | PDF |
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    Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design
    IEC 60601-1-9:2007 (EN-FR) forword
    Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design

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    • $ 220.99 232.62 | PDF |
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    Amendment 1 - Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design
    IEC 60601-1-9:2007/AMD1:2013 (EN-FR) forword
    Amendment 1 - Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design

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    Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems
    IEC 60601-1-8:2006+AMD1:2012 CSV (EN-FR) forword
    Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems

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    • $ 1,060.75 1,116.58 | PDF |
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    Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
    IEC 60601-1-11:2015+AMD1:2020 CSV (EN-FR) forword
    Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment

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    • $ 723.74 761.83 | PDF |
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    Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
    IEC 60601-1-6:2010+AMD1:2013+AMD2:2020 CSV (EN-FR) forword
    Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability

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    • $ 486.18 511.76 | PDF |
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    Amendment 1 - Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
    IEC 60601-1-11:2015/AMD1:2020 (EN-FR) forword
    Amendment 1 - Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment

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    • $ 22.10 23.26 | PDF |
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    Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
    IEC 60601-1-8:2006 (EN-FR) forword
    Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems

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    Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software
    IEC TR 80002-1:2009 forword
    Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software

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    Application of risk management for IT-networks incorporating medical devices - Part 2-9: Application guidance - Guidance for use of security assurance cases to demonstrate confidence in IEC TR 80001-2-2 security capabilities
    IEC TR 80001-2-9:2017 forword
    Application of risk management for IT-networks incorporating medical devices - Part 2-9: Application guidance - Guidance for use of security assurance cases to demonstrate confidence in IEC TR 80001-2-2 security capabilities

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    • $ 276.24 290.78 | PDF |
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    Application of risk management for IT-networks incorporating medical devices - Part 1: Safety, effectiveness and security in the implementation and use of connected medical devices or connected health software
    IEC 80001-1:2021 (EN-FR) forword
    Application of risk management for IT-networks incorporating medical devices - Part 1: Safety, effectiveness and security in the implementation and use of connected medical devices or connected health software

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    • $ 276.24 290.78 | PDF |
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    Application of risk management for IT-networks incorporating medical devices - Part 2-8: Application guidance - Guidance on standards for establishing the security capabilities identified in IEC TR 80001-2-2
    IEC TR 80001-2-8:2016 forword
    Application of risk management for IT-networks incorporating medical devices - Part 2-8: Application guidance - Guidance on standards for establishing the security capabilities identified in IEC TR 80001-2-2

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    • $ 353.58 372.19 | PDF |
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    Application of risk management for IT-networks incorporating medical devices - Part 2-5: Application guidance - Guidance on distributed alarm systems
    IEC TR 80001-2-5:2014 forword
    Application of risk management for IT-networks incorporating medical devices - Part 2-5: Application guidance - Guidance on distributed alarm systems

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    • $ 276.24 290.78 | PDF |
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    Application of risk management for IT-networks incorporating medical devices - Part 2-2: Guidance for the disclosure and communication of medical device security needs, risks and controls
    IEC TR 80001-2-2:2012 forword
    Application of risk management for IT-networks incorporating medical devices - Part 2-2: Guidance for the disclosure and communication of medical device security needs, risks and controls

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    • $ 353.58 372.19 | PDF |
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