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Cardiovascular Devices News

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76-90 of 2720 results
Creavo gets CE mark approval for Vitalscan portable medical device
By MDBR Staff Writer
UK-based medical device firm Creavo Medical Technologies has secured CE mark approval for its portable medical device, Vitalscan.
Specialty Devices > Cardiovascular Devices > News
European Commission conditionally approves Abbott's acquisition of St. Jude Medical
By MDBR Staff Writer
The European Commission (EC) has approved Abbott Laboratories' proposed $25bn acquisition of St Jude Medical.
Specialty Devices > Cardiovascular Devices > News
BioVentrix announces first clinical use of Revivent TC transcatheter ventricular enhancement system in Netherlands
BioVentrix announced the first clinical use in the Netherlands of its closed-chest Revivent TC™ transcatheter Ventricular Enhancement System.
Specialty Devices > Cardiovascular Devices > News
Medtronic new data demonstrates Heli-FX EndoAnchor system ehnahces outcomes and durability in complex aortic disease
Medtronic announced data demonstrating that the company's Heli-FX(TM) EndoAnchor(TM) system enhances outcomes and durability in patients with complex aortic abdominal aneurysm (AAA) anatomy, particularly those who have hostile aortic neck anatomy.
Specialty Devices > Cardiovascular Devices > News
HeartFlow FFRct Analysis receives regulatory approval in Japan
HeartFlow has announced the approval of its HeartFlow FFRct Analysis by the Japanese Ministry of Health, Labour and Welfare (MHLW).
Specialty Devices > Cardiovascular Devices > News
Millar signs clinical distribution agreement with Taisho Biomed Instruments
Millar, a leader in technology that enables scientific discovery and increased medical understanding, announced it has signed a distribution agreement with Taisho Biomed Instruments to market and sell the Millar Mikro-Cath Cardiovascular Pressure Catheter in Japan.
Specialty Devices > Cardiovascular Devices > News
Gore completes enrollment in Global Registry for Endovascular Aortic Treatment
W. L. Gore & Associates announced at the VEITHsymposium, the completion of target enrollment in the Global Registry for Endovascular Aortic Treatment (GREAT).
Specialty Devices > Cardiovascular Devices > News
FDA approves Medtronic’s Claria MRI CRT-D device to treat heart failure patients
By MDBR Staff Writer
The US Food and Drug Administration (FDA) has approved Medtronic's Claria MRI quad cardiac resynchronization therapy defibrillator (CRT-D) SureScan device to treat patients with heart failure.
Specialty Devices > Cardiovascular Devices > News
BIOTRONIK launches ultra-high energy ICD for heart failure patients
BIOTRONIK has launched Inventra HF-T, the first and only implantable cardioverter defibrillator (ICD) available in the US that delivers an ultra-high energy with 42 joules (J) on the first shock.
Specialty Devices > Cardiovascular Devices > News
St. Jude Medical gets CE mark for MRI labeling of Quadra Allure MP CRT-P
By MDBR Staff Writer
St. Jude Medical has secured CE mark approval for magnetic resonance (MR) conditional labeling of its Quadra Allure MP cardiac resynchronization therapy pacemaker (CRT-P).
Specialty Devices > Cardiovascular Devices > News
Boston Scientific announces initial US commercial performance of WATCHMAN LAAC device
Boston Scientific has announced initial U.S. commercial performance results of the WATCHMAN™ Left Atrial Appendage Closure (LAAC) Device at the 28th Transcatheter Cardiovascular Therapeutics (TCT), the annual scientific symposium of the Cardiovascular Research Foundation, in Washington, D.C.
Specialty Devices > Cardiovascular Devices > News
Cardinal Health to expand Cordis' cardiovascular product offerings in Asia Pacific
Cardinal Health has entered into two new distribution agreements that will enable Cordis, its interventional vascular business, to expand its cardiovascular portfolio in Asia Pacific.
Specialty Devices > Cardiovascular Devices > News
Bionet America introduces new Cardio7
Bionet America has launched new and improved Cardio7 (ECG), their latest addition to their ECG line.
Specialty Devices > Cardiovascular Devices > News
Shockwave Medical to begin study to target calcified lesions in peripheral arteries
Shockwave Medical has announced plans for DISRUPT PAD III, the largest ever multi-center randomized study to exclusively enroll patients with calcified peripheral artery disease (PAD).
Specialty Devices > Cardiovascular Devices > News
Cardiovascular Systems to start trial to study coronary atherectomy for calcified coronary lesions
By MDBR Staff Writer
Medical device firm Cardiovascular Systems (CSI) is set to start ECLIPSE clinical trial, which will study coronary atherectomy for calcified coronary lesions.
Specialty Devices > Cardiovascular Devices > News
76-90 of 2720 results