11.040.01 : Medical equipment in general

24/30506273 DC:2024

24/30506273 DC:2024

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BS EN IEC 60601-1/FRAG11 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - Electromagnetic exposure hazards (Fragment 11)

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24/30506277 DC:2024

24/30506277 DC:2024

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BS EN IEC 60601-1/FRAG2 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - Physical environment hazard (Fragment 2)

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24/30506281 DC:2024

24/30506281 DC:2024

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BS EN IEC 60601-1/FRAG3 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - User interface hazards (Fragment 3)

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24/30506285 DC:2024

24/30506285 DC:2024

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BS EN IEC 60601-1/FRAG4 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - Materials hazards (Fragment 4)

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DIN EN ISO 20417:2024-12

DIN EN ISO 20417:2024-12

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Medical devices - Information to be supplied by the manufacturer (ISO/DIS 20417:2024); German and English version prEN ISO 20417:2024

€179.53

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24/30500890 DC:2024

24/30500890 DC:2024

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BS EN ISO 20417 Medical devices - Information to be supplied by the manufacturer

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UNE-EN ISO 16571:2024

UNE-EN ISO 16571:2024

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Systems for evacuation of plume generated by medical devices (ISO 16571:2024)

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VDI-EE 5702 Blatt 3:2024-11

VDI-EE 5702 Blatt 3:2024-11

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Medical device software - Medical SPICE - Recommendations for software development

€153.15

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BS EN ISO 15378:2017+A1:2024

BS EN ISO 15378:2017+A1:2024

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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)

€404.00

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PR NF EN ISO 10993-17/A1 (10/2024)

PR NF EN ISO 10993-17/A1 (10/2024)

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Évaluation biologique des dispositifs médicaux - Partie 17 : Appréciation du risque toxicologique des constituants des dispositifs médicaux - Amendement 1

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BS EN IEC 60601-2-75:2019+A1:2024

BS EN IEC 60601-2-75:2019+A1:2024

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Medical electrical equipment Particular requirements for the basic safety and essential performance of photodynamic therapy diagnosis

€316.00

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BS 8684:2024

BS 8684:2024

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

€316.00

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BS EN IEC 80601-2-78:2020+A1:2024

BS EN IEC 80601-2-78:2020+A1:2024

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

€404.00

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UNE-EN ISO 15378:2018/A1:2024

UNE-EN ISO 15378:2018/A1:2024

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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 (ISO 15378:2017/Amd 1:2024)

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NBN EN ISO 15378:2017/A1:2024

NBN EN ISO 15378:2017/A1:2024

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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 (ISO 15378:2017/Amd 1:2024)

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