Initial data looking at safety and efficacy of an interatrial septal occluder with a bioresorbable frame show promise for closing atrial septal defects (ASDs), but the study authors suggest a redesign ...
The sponsor presented a decision tree (for the peri-procedural period) followed by a Markov model (for long-term outcomes) to estimate the costs and consequences associated with Pipeline against 5 ...
BOULDER, Colo., Nov. 10, 2025 /PRNewswire/ -- A woman in Delaware has become the first patient to undergo minimally invasive, endovascular surgery with a polymer-based coil. The coil, manufactured by ...
LONDON--(BUSINESS WIRE)--The need for quality patient care has increased owing to the growing aging population and the consequent rise in chronic diseases. Early diagnosis and regular monitoring of ...
Shape Memory Medical’s IMPEDE embolisation plug range has received CE mark as a Class III device under the European Union’s Medical Device Regulation (EU MDR). The US company’s embolisation plugs are ...
LONDON--(BUSINESS WIRE)--The global vascular embolization devices market is expected to grow by USD 1 billion during 2020-2024, progressing at a CAGR of almost 6% during the forecast period. The ...
GlobalData on MSN
FDA tags Medtronic embolisation device recall as Class I
The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...
NICE, the healthcare guidance body, today (30 May) issues guidance on an innovative medical technology device which can benefit patients with complex brain aneurysms - a bulging blood vessel in the ...
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