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Edwards Granted CE Mark For First Transcatheter Tricuspid Therapy

May 01, 2018

News Industry News

Eurocor announces the presentation of the 12 months data of the Freeway Stent Study at CIRSE in Copenhagen

September 19, 2017

News Industry News

Eurocor announces the completion of the Freeway Stent Study

April 04, 2017

News Industry News

CARDIONOVUM Announces Enrollment Completion of RAPID Trial

June 06, 2016

News Industry News

Medtronic Enrolls First Patients in Clinical Study to Evaluate the CoreValve(TM) Evolut(TM) R System in 'Real-World' Setting

March 06, 2016

News Industry News

Mitralign Percutaneous Annuloplasty System Earns CE Mark Approval for Functional Mitral Regurgitation

February 21, 2016

News Industry News

MValve Technologies Implants First Human Catheter Based Mitral Valve Replacement System

October 05, 2015

News Industry News

Medtronic Announces CE Mark for Recapturable CoreValve Evolut R System

September 03, 2014

News Industry News

Medtronic CoreValve® System Demonstrates Positive Clinical Performance at Two Years in 'Real World' ADVANCE Study

May 21, 2014

News Industry News

Medtronic Gains CE Mark for CoreValve® Evolut™ 23mm

September 26, 2012

News Industry News

Eurocor’s DEBIFU Registry successfully enrolled first patients

September 24, 2012

News Industry News

Cardionovum® expects to launch next-generation product: drug-eluting coronary stent system, PROLIMUS Biograde

August 08, 2012

News Industry News

Cardionovum® begins in vivo testing of its paclitaxel-coated RESTORE® drug-eluting balloon (DEB), designed to increase drug-in-tissue concentration

July 03, 2012

News Industry News

Eurocor GmbH announces presentation of Valentines Trial II results at CRT2012

February 07, 2012

News Industry News

Eurocor announces first insights of the Freeway Stent Study at LINC Congress

February 01, 2012

News Industry News

Eurocor announces treatment of First Patients in International Randomized Freeride Study

January 24, 2012

News Industry News

Eurocor’s DIOR DEB shows remarkable performance in diabetics with coronary lesions

November 10, 2011

News Industry News

InSeal Medical Announces Patients Successfully Treated with Novel Intravascular Large Bore Puncture Closure Device

November 08, 2011

News Industry News

Axxess Self-Expanding Bifurcation Drug-Eluting Stent Shown To Be Safe And Effective Up To Five Years

November 07, 2011

News Industry News

Mechanical chest compression device LUCAS may improve survival in PEA patients

February 14, 2011

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Edwards Granted CE Mark For First Transcatheter Tricuspid Therapy

Eurocor announces the presentation of the 12 months data of the Freeway Stent Study at CIRSE in Copenhagen

Eurocor announces the completion of the Freeway Stent Study

CARDIONOVUM Announces Enrollment Completion of RAPID Trial

Medtronic Enrolls First Patients in Clinical Study to Evaluate the CoreValve(TM) Evolut(TM) R System in 'Real-World' Setting

Mitralign Percutaneous Annuloplasty System Earns CE Mark Approval for Functional Mitral Regurgitation

MValve Technologies Implants First Human Catheter Based Mitral Valve Replacement System

Medtronic Announces CE Mark for Recapturable CoreValve Evolut R System

Medtronic CoreValve® System Demonstrates Positive Clinical Performance at Two Years in 'Real World' ADVANCE Study

Medtronic Gains CE Mark for CoreValve® Evolut™ 23mm

Eurocor’s DEBIFU Registry successfully enrolled first patients

Cardionovum® expects to launch next-generation product: drug-eluting coronary stent system, PROLIMUS Biograde

Cardionovum® begins in vivo testing of its paclitaxel-coated RESTORE® drug-eluting balloon (DEB), designed to increase drug-in-tissue concentration

Eurocor GmbH announces presentation of Valentines Trial II results at CRT2012

Eurocor announces first insights of the Freeway Stent Study at LINC Congress

Eurocor announces treatment of First Patients in International Randomized Freeride Study

Eurocor’s DIOR DEB shows remarkable performance in diabetics with coronary lesions

InSeal Medical Announces Patients Successfully Treated with Novel Intravascular Large Bore Puncture Closure Device

Axxess Self-Expanding Bifurcation Drug-Eluting Stent Shown To Be Safe And Effective Up To Five Years

Mechanical chest compression device LUCAS may improve survival in PEA patients

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