The CE Marking approval indicates that a medical device meets the requirements of the European Medical Devices Directive. Until now, Materialise’s personalized devices made use of the custom-made ...
Certification of Hexadrone’s TUNDRA 2.1 by Applus+ Laboratories confirms compliance with EU Regulation 2019/945 and stre ...
SEATTLE--(BUSINESS WIRE)--Tasso, Inc., the leading provider of patient-centric clinical-grade blood collection solutions, today announced it received CE Mark certification for its Tasso+™ device, a ...
The Revivent TC™TransCatheter Ventricular Enhancement System enables the treatment and management of patients who suffered a myocardial infarction resulting in left ventricular dysfunction SAN RAMON, ...
Certification opens the European market for the first FDA-cleared AI platform for prostate MRI interpretation. OMAHA, Neb., Oct. 27, 2025 /PRNewswire/ -- Bot Image, Inc., a leader in AI-powered ...
ZHENJIANG, JIANGSU, CHINA, January 8, 2026 /EINPresswire.com/ -- The modern eyewear market is a dynamic convergence of ...
Please provide your email address to receive an email when new articles are posted on . BTG received Class III CE Mark certification for its DC Bead LUMI, a radiopaque drug-eluting bead for patients ...