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    I.S. EN IEC 60601-2-31:2020

    Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source (IEC 60601-2-31:2020)

    National Standards Authority of Ireland

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    I.S. EN IEC 80601-2-60:2020

    Medical electrical equipment - Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment (IEC 80601-2-60:2019)

    National Standards Authority of Ireland

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    I.S. EN 13718-2:2015+A1:2020

    MEDICAL VEHICLES AND THEIR EQUIPMENT - AIR AMBULANCES - PART 2: OPERATIONAL AND TECHNICAL REQUIREMENTS FOR AIR AMBULANCES

    National Standards Authority of Ireland

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    I.S. EN 13718-1:2014+A1:2020

    Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances

    National Standards Authority of Ireland

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    I.S. EN ISO 14971:2019

    Medical devices - Application of risk management to medical devices (ISO 14971:2019)

    National Standards Authority of Ireland

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    I.S. EN 60601-2-75:2019

    Medical Electrical Equipment - Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment

    National Standards Authority of Ireland

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    ISO 10993-2 : 2006(R2015)

    BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 2: ANIMAL WELFARE REQUIREMENTS

    International Organization for Standardization

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    I.S. EN ISO 13485:2016&LC:2016&AC:2018

    Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)

    National Standards Authority of Ireland

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    I.S. EN IEC 80601-2-30:2019

    Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers (IEC 80601-2-30:2018)

    National Standards Authority of Ireland

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    SR CEN/TR 17223:2018

    GUIDANCE ON THE RELATIONSHIP BETWEEN EN ISO 13485: 2016 (MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - REQUIREMENTS FOR REGULATORY PURPOSES) AND EUROPEAN MEDICAL DEVICES REGULATION AND IN VITRO DIAGNOSTIC MEDICAL DEVICES REGULATION

    National Standards Authority of Ireland