11.040.01 : Medical equipment in general

IEC TS 60601-4-6:2024

IEC TS 60601-4-6:2024

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Medical electrical equipment - Part 4-6: Guidance and interpretation - Voluntary guidance to help achieve basic safety and essential performance with regard to the possible effects of electromagnetic disturbances

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PD IEC TS 60601-4-2:2024

PD IEC TS 60601-4-2:2024

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Medical electrical equipment Guidance and interpretation. Electromagnetic immunity: performance of medical systems

€374.00

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NF EN 60601-1/A13, C74-011/A13 (04/2024)

NF EN 60601-1/A13, C74-011/A13 (04/2024)

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Appareils électromédicaux - Partie 1 : exigences générales pour la sécurité de base et les performances essentielles

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24/30475124 DC:2024

24/30475124 DC:2024

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BS EN ISO 11197 Medical supply units

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IEC TS 60601-4-2:2024

IEC TS 60601-4-2:2024

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IEC TS 60601-4-2:2024 Medical electrical equipment - Part 4-2: Guidance and interpretation - Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems

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ASTM F3438-24

ASTM F3438-24

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Standard Guide for Detection and Quantification of Cleaning Markers (Analytes) for the Validation of Cleaning Methods for Reusable Medical Devices

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IEC 80601-2-78:2019+AMD1:2024 Consolidated

IEC 80601-2-78:2019+AMD1:2024 Consolidated

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Medical electrical equipment - Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation

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IEC 80601-2-78:2019/AMD1:2024

IEC 80601-2-78:2019/AMD1:2024

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Amendment 1 - Medical electrical equipment - Part 2-78: Particular requirements for basic safety and essential performance of medical robots for rehabilitation, assessment, compensation or alleviation

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NF EN 302195, Z84-195 (03/2024)

NF EN 302195, Z84-195 (03/2024)

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Dispositifs à courte portée (SRD) - Implants médicaux actifs de puissance ultra basse (ULP-AMI) et accessoires (ULP-AMI-P) fonctionnant dans la plage de fréquences de 9 kHz à 315 kHz - Norme harmonisée couvrant les exigences essentielles de l'article 3, paragraphe 2, de la Directive 2014/53/UE (V2.1.1)

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ISO 15378:2017/Amd 1:2024

ISO 15378:2017/Amd 1:2024

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Primary packaging materials for medicinal products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) Amendment 1: Climate action changes

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IEC 80601-2-26:2019/AMD1:2024

IEC 80601-2-26:2019/AMD1:2024

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Amendment 1 - Medical electrical equipment - Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs

€22.00

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IEC 80601-2-26:2019+AMD1:2024 Consolidated

IEC 80601-2-26:2019+AMD1:2024 Consolidated

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Medical electrical equipment - Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs

€528.00

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24/30450887 DC:2024

24/30450887 DC:2024

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BS 8684. Technology enabled care. Assessment of user needs and risks, system design, installation and maintenance. Code of practice

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BS EN IEC 60601-2-35:2021+A1:2024

BS EN IEC 60601-2-35:2021+A1:2024

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Medical electrical equipment Particular requirements for the basic safety and essential performance of heating devices using blankets, pads or mattresses intended in medical use

€404.00

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BS EN IEC 80601-2-77:2021+A1:2023

BS EN IEC 80601-2-77:2021+A1:2023

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Medical electrical equipment Particular requirements for the basic safety and essential performance of robotically assisted surgical

€374.00

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