Tag: Regulation (EU) 2017/745

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Recent Related Articles to Regulation (EU) 2017/745

New EU Responsibility and Liability Landscape for Smart Medical Devices in a Global Context

Added to Collection on: 2025-07-22 15:41:32

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Regulation of medical devices
Regulation of artificial intelligence
Regulation (EU) 2017/745
Medical device
Notified body
Artificial Intelligence Act
Artificial intelligence
Regulation (EU) 2017/746
Tort
Regulation (EU) 2023/988
Regulatory compliance
Product liability

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SurgiBox Achieves CE Mark for SurgiField System Devices to Improve Access to Safe ...

Added to Collection on: 2025-08-07 16:27:11

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Health care
Medical device
Regulation (EU) 2017/745
Surgery
Medicine
Outpatient surgery
SurgiBox Inc.
Cambridge

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UV Device Confusion: Why Hospitals Must Ask the Right Regulatory Questions

Added to Collection on: 2025-08-07 18:08:27

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Food and Drug Administration
Hygiene
Ultraviolet radiation
Food law
Medical devices
Medical device
Federal Food, Drug, and Cosmetic Act
Ultraviolet
Disinfectant
Regulation (EU) 2017/745
Single Use Medical Device Reprocessing
Gunner Lyslo

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Emerging Markets Are Pioneering Hybrid Clinical Trial Models For Medtech Products

Added to Collection on: 2025-08-25 15:21:36

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Health informatics
Clinical research
Regulation of medical devices
Clinical trial
Design of experiments
Regulation (EU) 2017/745
Digital health
Medical device
CLARIO
Telehealth
Julio G. Martinez-Clark

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Nuon Medical elevates cosmetic packaging into smart technology - Premium Beauty News

Added to Collection on: 2025-09-15 23:28:25

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Skin care
Regulation of medical devices
Health care
Medical device
Beauty
Collagen induction therapy
Light therapy
Regulation (EU) 2017/745

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European Union calls for evidence on simplifying medical device rules - JD Supra

Added to Collection on: 2025-09-17 20:24:51

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Regulation of medical devices
Regulation (EU) 2017/746
Regulation (EU) 2017/745
Medical device
MDR
Artificial Intelligence Act
CE marking
Regulation (EU) No. 305/2011
European authorised representative
Postmarketing surveillance

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Successful ISO 13485 Certification Paves the way for Market Launch of ViroCAP(R) in October 2025

Added to Collection on: 2025-09-18 22:06:40

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Regulation of medical devices
ISO 13485
Medical device
Regulation (EU) 2017/745
Dermatology
D. Medical Industries
Viromed Medical AG

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Neuromod Advance Multiple Regulatory Approvals to Expedite Global Availability of Lenire

Added to Collection on: 2025-09-23 04:41:36

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Audiology
Psychoacoustics
Neurotechnology
Symptoms
Tinnitus
Medical device
Neuromodulation
Regulation (EU) 2017/745
Tinnitus masker
Tinnitus retraining therapy
Neuromod Devices

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FormlyAI: $2 Million Raised For Medical Device Certification Solution

Added to Collection on: 2025-09-22 16:43:34

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Regulation of medical devices
Cybernetics
Health care
Medical device
Artificial intelligence
Regulation (EU) 2017/745
Startup company
Draft:Developair Technologies
FormlyAI

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Neuromod Regulatory Approvals to Improve Lenire Global Availability | The Hearing Review

Added to Collection on: 2025-10-01 03:38:25

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Regulation of medical devices
Regulation (EU) 2017/745
Medical device
Tinnitus
ISO 13485
Food and Drug Administration
Regulation (EU) 2017/746
Regulatory compliance
Single Use Medical Device Reprocessing
Design controls

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