WEIFANG, SHANDONG, CHINA, January 29, 2026 /EINPresswire.com/ -- In the current global industrial landscape, energy ...
Lumea’s Viewer+™ software is now CE marked under IVDR for clinical use across Europe, making Lumea the most versatile ...
Q4 2025 earnings call: nsPFA clinical/regulatory timeline, Vybrance rollout, revenue trends, cash burn & outlook—read now.
Zoll announced today that it received CE mark approval under European Medical Device Regulation (MDR) for its Zenix ...
The Medicines and Healthcare products Regulatory Agency (MHRA) is hoping to address a critical regulatory issue for medical ...
CE Mark certification enables commercialization across Europe and other CE-recognizing marketsClinical evidence from a 121-patient prospective study supports device safety and efficacyCertification ...
Paris, January 26, 2026 – HighLife SAS, a leading MedTech company focused on transcatheter solutions for structural heart disease, today announced that it has received CE Mark approval for the ...
InVera Medical, an Irish medical technology company, has received European regulatory approval for a new minimally invasive device designed to ...
InVera Medical’s new vein infusion device receives European CE Mark approval: Galway, Ireland Monday, February 16, 2026, 12:00 Hrs [IST] InVera Medical, an Irish medical technol ...