The Council of the European Union has published a second set of corrections as part of a corrigendum for the EU’s Medical Devices Regulation (MDR), this time giving manufacturers of certain Class I ...
Dublin, Nov. 03, 2023 (GLOBE NEWSWIRE) -- The "Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations" conference has been added to ResearchAndMarkets.com's offering. This ...
As part of its efforts to regulate the medical devices in the country, the Drugs Controller General (India) has issued a notice classifying 48 medical devices pertaining to oncology under the ...
P&F Products and Features GmbH, a global heart valve MedTech company focused on transcatheter solutions for structural heart ...
Under MDR, devices addressing sleep-related conditions—particularly those involving neuromuscular stimulation—are subject to classification, safety assessment, and performance documentation.
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