11.040.01 : Medical equipment in general

25/30513264 DC:2025

25/30513264 DC:2025

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BS EN ISO 16571:2024/Amd 1 Systems for evacuation of plume generated by medical devices. Amendment 1

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IEC 61847:2025

IEC 61847:2025

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Ultrasonics - Surgical systems - Measurement and declaration of the basic output characteristics

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25/30510717 DC:2025

25/30510717 DC:2025

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Draft BS EN 63612 Ultrasonics. Intraluminal short pressure pulse therapy sources. Characteristics of fields

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25/30500985 DC:2025

25/30500985 DC:2025

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Draft BS EN 63521 Machine Learning-enabled Medical Device. Performance Evaluation Process

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PR NF EN ISO 10993-3, S99-501-3PR (05/2025)

PR NF EN ISO 10993-3, S99-501-3PR (05/2025)

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Évaluation biologique des dispositifs médicaux - Partie 3 : Évaluation de la génotoxicité, de la cancérogénicité, de la toxicité sur la reproduction et le développement

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PR NF EN ISO 10993-11, S99-501-11PR (05/2025)

PR NF EN ISO 10993-11, S99-501-11PR (05/2025)

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Évaluation biologique des dispositifs médicaux - Partie 11 : Essais de toxicité systémique

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UNE-CEN ISO/TR 24971:2025 IN

UNE-CEN ISO/TR 24971:2025 IN

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Medical devices - Guidance on the application of ISO 14971 (ISO/TR 24971:2020)

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ISO 15223-1:2021/Amd 1:2025

ISO 15223-1:2021/Amd 1:2025

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Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific

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NF EN ISO 10993-5/A11, S99-501-5/A11 (03/2025)

NF EN ISO 10993-5/A11, S99-501-5/A11 (03/2025)

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Évaluation biologique des dispositifs médicaux - Partie 5 : essais concernant la cytotoxicité in vitro

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25/30453854 DC:2025

25/30453854 DC:2025

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BS EN IEC 80601-2-30. Medical electrical equipment Part 2-30. Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers

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FD T90-525 (02/2025)

FD T90-525 (02/2025)

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Qualité de l'eau - Guide technique d'échantillonnage pour le suivi de la qualité des eaux de soins hospitalières, des fluides d'hémodialyse, du contrôle sur dispositif médical et des eaux minérales naturelles utilisées à des fins thérapeutiques

€156.67

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NF EN ISO 10993-4/A1, S99-501-4/A1 (02/2025)

NF EN ISO 10993-4/A1, S99-501-4/A1 (02/2025)

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Évaluation biologique des dispositifs médicaux - Partie 4 : choix des essais pour les interactions avec le sang - Amendement 1

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25/30502360 DC:2025

25/30502360 DC:2025

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BS EN IEC 62304 Health software – Software life cycle processes

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PR NF EN ISO 20417, S99-001PR (01/2025)

PR NF EN ISO 20417, S99-001PR (01/2025)

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Dispositifs médicaux - Informations à fournir par le fabricant

This product is not for sale, please contact us for more information

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24/30506269 DC:2024

24/30506269 DC:2024

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BS EN IEC 60601-1/FRAG1 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - (Fragment 1)

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