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IEC 60601 Updates: What MedTech Need to Know for 2025 and Beyond Podcast

In this episode of the Global Medical Device Podcast, Etienne Nichols sits down with Leo Eisner, founder of Eisner Safety Consultants and a leading voice in IEC 60601 standards development. We unpack the upcoming revisions to IEC 60601, 4th ed.,

leoeisner December 12, 2024December 12, 2024 10993, 13485, 14971, 15223-1, 20417, 60601 Series, 60601-1, 60601-1-10, 60601-1-11, 60601-1-12, 60601-1-2, 60601-1-6, 60601-1-8, 60601-1, 4th edition, 62304, 62366, 62366-1, Alarm Systems, Architecture Specification, Coexistence, Dec 2024, Design Specification, Device, EMC, Essential Performance, FDA, Greenlight Guru, Guidance Documents, Hazards, IEC, IEC 60601-1, Information provided by the manufacturer, Ionizing radiation, ISO 10993, ISO 13485, ISO 15223-1, ISO 20417, Labeling, London, Marking, Mechanical, Medical Device, PEMS, Physiologic Closed-Loop Control, Podcast, Recognized Consensus Standards, Regulation, Regulatory Affairs, Risk Management, SaMD, Scotland, SiMD, Software, Standards, Standards Development, State of the Art, UK, US, Usability, Usability Engineering Process Read more

Regulatory Updates – January 2022

Regulatory Update – January 2022 Index I have 4 Regulatory updates (US (2), England, Scotland & Wales (1), EU 1)) for you that are full of great information. Below is a mini index so you can jump around the world

leoeisner January 31, 2022June 12, 2022 Active Implants, Brexit, Combination Product, Computational Modeling, Computational Simulation, Designated Standards, Device, Draft Guidance, FDA, Final Guidance, Guidance Documents, Hamonised Standards, IVD, IVDR, Jan 2022, MDR, Medical Device Regulation, Patient Engagement, Patient Reported Outcome Instruments for Use in Medical Device Evaluation, Physiologic Closed-Loop Control, Recognized Consensus Standards, Reprocessing, Scotland, Software, Standards, UDI, UK, Wales Read more

Categories – Drop Down

Categories – Hot Topics

510(k) 60601 series 60601-1 60601-1 3rd ed. A1 AAMI AAMI ES60601-1 AAMI ES60601-1/C1 Active Implantable Medical Devices Directive AIMDD Amendment 1 ANSI/AAMI ES60601-1 CDRH CENELEC Collateral Standard EN60601 EN60601-1 ESCNews EU European Commission FDA FDA Guidance Health Canada Home Healthcare Environments Home Use Home Use Environment Home Use Med Dvcs IEC IEC 60601-1 IEC60601-1 IEC60601-1 3rd ed. IEC60601-1-11 ISO 14971 IVD IVDD MDD MDD Amendment Medical Medical Device Medical Device Directive Medical Device Industry Medical Device Regulatory Medical Devices Notified Body Risk Management

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