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Venusp-Valve(TM) Obtains Ce Marking Under MDR and Debuts in Europe as China’s First Valve Product

On April 8th, 2022, VenusP-ValveTM, Venus Medtech's in-house developed innovative transcatheter pulmonic valve replacement (TPVR) system, received CE marking under the Medical Devices Regulation...

GlobalMed Announces Compliance with European Medical Device Regulation (MDR)

GlobalMed, an international provider of virtual health solutions, is proud to announce that its eNcounter® telehealth software suite, ClinicalAccess® Station Lite and multiple diagnostic...
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