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1-15 of 3094 results
Shockwave Medical gets CE mark for Coronary Lithoplasty system
By MDBR Staff Writer
Shockwave Medical has secured CE mark for its Coronary Lithoplasty system to treat calcified plaque in conjunction with stenting in patients with coronary artery disease.
Specialty Devices > Cardiovascular Devices > News
Boston Scientific receives US FDA approval For Resonate family of high-voltage devices
Boston Scientific has received US Food and Drug Administration (FDA) approval for the Resonate family of implantable cardioverter defibrillator (ICD) and cardiac resynchronization therapy defibrillator (CRT-D) systems.
Specialty Devices > Cardiovascular Devices > News
Abbott gets CE mark for smartphone compatible insertable cardiac monitor
Abbott has secured CE mark approval for its new Confirm Rx insertable cardiac monitor (ICM), the world's first smartphone compatible ICM that will help physicians identify difficult to detect cardiac arrhythmias, including atrial fibrillation (AF), to help guide therapy.
Specialty Devices > Cardiovascular Devices > News
Medtronic recalls StrataMR adjustable valves and shunts
Medtronic has announced that on 22 February, 2017 it notified customers of a voluntary recall of all unused units of the StrataMR adjustable valves and shunts.
Specialty Devices > Cardiovascular Devices > News
Cardiovascular Systems gets approval for Diamondback 360 OAS Micro Crown system in US
Cardiovascular Systems announced that the US Food and Drug Administration (FDA) has approved the Diamondback 360 Coronary orbital atherectomy system (OAS) Micro Crown system to facilitate stent delivery in patients with coronary artery disease (CAD) who are acceptable candidates for PTCA or stenting due to de novo, severely calcified coronary artery lesions.
Specialty Devices > Cardiovascular Devices > News
Boston Scientific to buy Swiss firm Symetis for $435m
By MDBR Staff Writer
Boston Scientific has agreed to acquire Switzerland-based medical technology firm Symetis for around $435m in cash.
Specialty Devices > Cardiovascular Devices > News
FDA approves Medtronic’s CoreValve Evolut PRO Valve for severe aortic stenosis
By MDBR Staff Writer
Medtronic has secured approval from the US Food and Drug Administration (FDA) for its CoreValve Evolut Pro transcatheter valve to treat severe aortic stenosis.
Specialty Devices > Cardiovascular Devices > News
1-15 of 3094 results