P&F Products and Features GmbH, a global heart valve MedTech company focused on transcatheter solutions for structural heart ...
Medical devices with valid certifications under the Medical Device Directive (MDD) will have to prepare to adapt to the incoming Medical Devices Regulation (MDR), particularly for up-classified ...
DentalMonitoring is proud to announce that the DentalMonitoring Software is now certified under the European Union Medical Device Regulation 2017/745 (EU MDR) and fulfills the requirements for CE ...
SHENZHEN, China--(BUSINESS WIRE)--As officially stated by EU Parliament on April 17, 2020, the Parliament decided to postpone the application date (May 26, 2020) of new requirements for medical ...
PARIS--(BUSINESS WIRE)--Regulatory News: CARMAT (FR0010907956, ALCAR), designer and developer of the world’s most advanced total artificial heart, aiming to provide a therapeutic alternative for ...
The "3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS" training has been added to ResearchAndMarkets.com's offering. This webinar will examine ...
Magstim Passes Compliance with Strict European Union Medical Device Regulations Expanding Magstim Access to Entire EU Marketplace WHITLAND, United Kingdom, May 16, 2025 (GLOBE NEWSWIRE) -- Magstim has ...
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