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Medtronic Announces CE Mark of Evolut™ PRO+ TAVI System for Treatment of Symptomatic Severe Aortic Stenosis Patients in Europe
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As TAVI Patient Population Grows, PRO+ TAVI System Launches with Four Valve Sizes and Lowest Delivery Profile
DUBLIN, May 3, 2021 /PRNewswire/ Medtronic plc (NYSE: MDT), the global leader in medical technology, today announced CE (Conformité Européenne) Mark of the Evolut™ PRO+ TAVI System – the newest-generation Medtronic TAVI system that builds off the proven self-expanding, supra-annular Evolut TAVI platform. The Evolut PRO+ TAVI System includes four valve sizes with an external pericardial tissue wrap that provides advanced sealing for the largest annular range (for self-expanding TAVI technology) on the market. The approval follows a recent indication expansion for the Evolut platform in Europe for patients with severe aortic stenosis who are at a low risk of surgical mortality and pa
Medtronic Announces CE Mark of Evolut PRO+ TAVI System for Treatment of Symptomatic Severe Aortic Stenosis Patients in Europe
As TAVI Patient Population Grows, PRO+ TAVI System Launches with Four Valve Sizes and Lowest Delivery Profile – Medtronic plc the global leader in medical technology, today announced CE Mark of the Evolut™ PRO+ TAVI System the newest-generation Medtronic TAVI system that builds off the proven self-expanding, supra-annular Evolut TAVI platform. The Evolut PRO+ TAVI System includes four valve sizes with an external … As TAVI Patient Population Grows, PRO+ TAVI System Launches with Four Valve Sizes and Lowest Delivery Profile
– Medtronic plc (NYSE: MDT), the global leader in medical technology, today announced CE (Conformité Européenne) Mark of the Evolut™ PRO+ TAVI System the newest-generation Medtronic TAVI system that builds off the proven self-expanding, supra-annular Evolut TAVI platform. The Evolut PRO+ TAVI System includes four valve siz
Scientific American
Researchers are searching for possible links between unusual clotting and the Oxford-AstraZeneca coronavirus vaccine
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The very rare occurrence of a mysterious blood-clotting disorder among some recipients of the Oxford–AstraZeneca COVID-19 vaccine has researchers scrambling to uncover whether and how the inoculation could trigger such an unusual reaction.
After weeks of investigation, the European Medicines Agency (EMA) announced on 7 April that there is a possible link between the clots and the vaccine. Even so, the clotting disorder described today in two reports in
The New England Journal of Medicine is so uncommon that the benefits of the vaccine still outweigh its risks, EMA executive director Emer Cooke told reporters. “These are very rare side effects,” she said. “The risk of mortality from COVID is much greater than the risk of mortality from these side effects.”
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