Cynosure Lutronic has announced CE Mark approval under the European Medical Device Regulation (MDR) for its Mosaic 3D ...
Highlife SAS secured CE mark for its transcatheter mitral valve replacement (TMVR) system, bringing a much needed treatment ...
In its letter to the European Commission, the European Organisation of Technical Assessment (EOTA) and stakeholders in the construction sector, the ERC advocates the adoption of CE marking through the ...
GE HealthCare (Nasdaq: GEHC) announced today that it received FDA 510(k) clearance and CE mark for its Allia Moveo platform.
Medtronic announced two new milestones for its Affera Sphere-360 catheter for pulsed field ablation (PFA) procedures.
HighLife Receives CE Mark Approval for its TMVR SolutionParis, January 26, 2026 – HighLife SAS, a leading MedTech company focused on ...
Fetoly is a real-time AI solution providing standardised foetal ultrasound examinations in accordance with ISUOG guidelines.
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GEHC wins FDA clearance & CE mark for Allia Moveo, marks global debut
GE HealthCare Technologies Inc. GEHC recently announced that it has obtained FDA 510(k) clearance and CE Marking for its ...
The Tribune, now published from Chandigarh, started publication on February 2, 1881, in Lahore (now in Pakistan). It was started by Sardar Dyal Singh Majithia, a public-spirited philanthropist, and is ...
GE HealthCare announced that its Allia Moveo imaging platform for the interventional suite has received FDA 510(k) clearance an ...
GE HealthCare (Nasdaq: GEHC) today announced that Allia™ Moveo has received U.S. Food and Drug Administration (FDA) 510(k) clearance and CE Marking, bringing next-level mobility and precision to the ...
The CE Mark certification enables Seno Medical to market and sell the latest version of its Imagio Imaging System with opto-acoustic, sound, and artificial intelligence in the European Union.SAN ...
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