making new medical technologies available in Hungary

From the 2018 Guidelines for the Early Management of Patients With Acute Ischemic Stroke

From the 2018 Guidelines for the Early Management of Patients With Acute Ischemic Stroke The 2018 Acute Ischemic Stroke (AIS) Guideline provides an up-to-date, comprehensive set of recommendations for clinicians caring for adult patients with AIS. Working jointly with the American Heart...
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Five-year Follow-up Data Demonstrate the WATCHMAN™ Left Atrial Appendage Closure Device Provides Stroke Risk Reduction Comparable to Warfarin Therapy

Five-year Follow-up Data Demonstrate the WATCHMAN™ Left Atrial Appendage Closure Device Provides Stroke Risk Reduction Comparable to Warfarin Therapy Late-breaking Clinical Trial Data Presented at TCT 2017 with Simultaneous Publication in the Journal of the American College of Cardiology Nov 2,...
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New Data from PLATINUM Diversity Study Presented at SCAI 2017 Provide Important Insights Beyond Traditional Clinically-Reported Endpoints

New Data from PLATINUM Diversity Study Presented at SCAI 2017 Provide Important Insights Beyond Traditional Clinically-Reported Endpoints Analyses Evaluated the Impact of Ethnicity, Gender and Income on Cardiovascular Outcomes May 12, 2017 NEW ORLEANS and MARLBOROUGH, Mass., May 12...
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SYNERGY™ BP Stent Demonstrates Excellent Safety in the EVOLVE II Clinical Trial Outstanding Safety in 18,000 Patients Across 9 Studies

Addressing the Full Spectrum of Cardiovascular Disease Complexity The SYNERGY™ Bioabsorbable Polymer (BP) Stent is being studied in 20 investigator-sponsored research trials including more than 30,000 patients, allowing physicians worldwide to provide data on patients receiving the SYNERGY BP...
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Long-term Safety with the SYNERGY Stent System

Long-term Safety with the SYNERGY Stent System EVOLVE II Trial 2-Year Results Dr. Dean Kereiakes highlights the key 2-Year data coming out of the EVOLVE II Trial including exceptionally low ST rates for the SYNERGY Stent System. Source: Boston Scientific
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Eluvia™ Drug-eluting Vascular Stent System Demonstrates 12-month Primary Patency Of 96.1 Percent

28 Sep 2015 MAJESTIC Trial Data Support Strong Safety Profile with Low Target Lesion Revascularization Rate MARLBOROUGH, Mass. – New 12-month clinical trial outcomes assessing the safety and performance of the Boston Scientific Eluvia™ Drug-Eluting Vascular Stent System reflect a primary...
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Boston Scientific receives CE mark for Eluvia™ drug-eluting vascular stent and announces initiation of new clinical trial

22 Feb 2016 First polymer-based, drug-eluting stent designed to treat peripheral lesions above the knee approved in Europe; IMPERIAL trial initiated to seek regulatory approvals in U.S. and Asia Boston Scientific, today announced that the Eluvia™ Drug-Eluting Vascular Stent System has received...
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Tryton Medical Announces Publication of Post Hoc Analysis of Randomized Clinical Trial in Treatment of Bifurcation Lesions using Tryton Side Branch Stent

Analysis showed reductions in target vessel failure and improved side branch percent diameter stenosis in patients with a coronary bifurcation lesion in vessels 2.25mm in diameter or greater September 30, 2015 06:30 AM Eastern Daylight Time DURHAM, N.C.–(BUSINESS WIRE)–Tryton...
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News Releases Eluvia™ Drug-eluting Vascular Stent System Demonstrates 12-month Primary Patency Of 96.1 Percent

MAJESTIC Trial Data Support Strong Safety Profile with Low Target Lesion Revascularization Rate Sep 28, 2015 MARLBOROUGH, Mass., Sept. 28, 2015 /PRNewswire/ — New 12-month clinical trial outcomes assessing the safety and performance of the Boston Scientific (NYSE: B...
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