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Cardiovascular Devices News

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91-105 of 2729 results
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
Fresenius Medical Care to buy medical technology firm Xenios
By MDBR Staff Writer
Fresenius Medical Care has agreed to acquire medical technology firm Xenios from German private venture capitalist zfhn Zukunftsfonds Heilbronn.
Specialty Devices > Cardiovascular Devices > News
Abiomed gets FDA IDE approval to start DTU study with Impella CP heart pump
By MDBR Staff Writer
Abiomed has secured investigational device exemption (IDE) approval from the US Food and Drug Administration (FDA) to start door to unloading (DTU) study with Impella CP heart pump.
Specialty Devices > Cardiovascular Devices > News
FDA approves St. Jude's PFO occlusion device for recurrent stroke risk reduction
By MDBR Staff Writer
St. Jude Medical has secured approval from the US Food and Drug Administration (FDA) for its new medical device indicated to reduce the risk of recurrent ischemic strokes in patients with a patent foramen ovale (PFO).
Specialty Devices > Cardiovascular Devices > News
FDA approves BioTrace Medical's temporary pacing technology
The US Food and Drug Administration (FDA) has approved BioTrace Medical's temporary pacing technology for transcatheter aortic valve procedures (TAVR) and other cardiovascular applications.
Specialty Devices > Cardiovascular Devices > News
St. Jude Medical shareholders approve merger with Abbott
The shareholders of St. Jude Medical have approved the merger with Abbott.
Specialty Devices > Cardiovascular Devices > News
FDA approves Medtronic's new recaptureable transcatheter aortic valve replacement system
By MDBR Staff Writer
Medtronic has secured approval from the US Food and Drug Administration (FDA) for its new CoreValve Evolut R 34 mm transcatheter aortic valve replacement (TAVR) system.
Specialty Devices > Cardiovascular Devices > News
91-105 of 2729 results