11.040.01 : Medical equipment in general

DIN EN ISO 18969:2026-01

DIN EN ISO 18969:2026-01

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Clinical evaluation of medical devices (ISO/DIS 18969:2025); German and English version prEN ISO 18969:2025

€134.02

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VDI 5702 Blatt 1:2026-01

VDI 5702 Blatt 1:2026-01

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Medical device software - Medical SPICE - Process assessment model

€307.20

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25/30551597 DC:2025

25/30551597 DC:2025

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Draft BS IEC 60601-1/FRAG4 ED4 Medical electrical equipment

€24.00

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ISO/DIS 18969:2025

ISO/DIS 18969:2025

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Clinical evaluation of medical devices

€77.00

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25/30466216 DC:2025

25/30466216 DC:2025

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BS EN ISO 18969 Clinical evaluation of medical devices

€24.00

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25/30510772 DC:2025

25/30510772 DC:2025

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Draft BS EN IEC 80601-2-77 ED2 Medical electrical equipment Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical

€24.00

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25/30510776 DC:2025

25/30510776 DC:2025

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Draft BS EN IEC 80601-2-78 ED2 Medical electrical equipment Part 2-78: Particular requirements for basic safety and essential performance of medical robots rehabilitation, assessment, compensation or alleviation

€24.00

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BS EN ISO 15223-1:2021+A1:2025

BS EN ISO 15223-1:2021+A1:2025

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Medical devices — Symbols to be used with information supplied by the manufacturer Part 1: General requirements

€421.00

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PD ISO/TS 4452:2025

PD ISO/TS 4452:2025

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Specification and demonstration of system reliability of single-use drug delivery systems

€281.00

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BS EN ISO 15223-1:2021+A1:2025 (CD-ROM+PDF)

BS EN ISO 15223-1:2021+A1:2025 (CD-ROM+PDF)

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Medical devices. Symbols to be used with information to be supplied by the manufacturer

€438.00

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ISO/TS 4452:2025

ISO/TS 4452:2025

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Specification and demonstration of system reliability of single-use drug delivery systems

€115.00

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NBN EN ISO 15223-1:2021/A1:2025

NBN EN ISO 15223-1:2021/A1:2025

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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 (ISO 15223 1:2021/Amd 1:2025)

€20.00

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BS EN ISO 15223-1:2021+A1:2025 CD-ROM

BS EN ISO 15223-1:2021+A1:2025 CD-ROM

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Medical devices - Symbols to be used with information supplied by the manufacturer Part 1: General requirements

€172.00

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UNE-EN ISO 14155:2021/A11:2025

UNE-EN ISO 14155:2021/A11:2025

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Clinical investigation of medical devices for human subjects - Good clinical practice

€59.00

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NF EN ISO 15223-1/A1, S99-014-1/A1 (11/2025)

NF EN ISO 15223-1/A1, S99-014-1/A1 (11/2025)

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Dispositifs médicaux - Symboles à utiliser avec les informations à fournir par le fabricant - Partie 1 : exigences générales - Amendement 1 : ajout du terme défini représentant autorisé (mandataire) et modification du symbole EC REP pour ne pas être spécifique d'un pays ou d'une région

€103.00

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