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1-15 of 2980 results
FDA approves LivaNova’s Memo 4D semi-rigid mitral annuloplasty ring
By MDBR Staff Writer
UK-based medical technology firm LivaNova has secured 510(k) clearance from the US Food and Drug Administration (FDA) for its Memo 4D semi-rigid mitral annuloplasty ring.
Specialty Devices > Cardiovascular Devices > News
CardioNXT, AFTx complete enrollment in RADAR clinical trial
Medical devices firms CardioNXT and AFTx announce that the real-time electrogram analysis for drivers of atrial fibrillation (RADAR) clinical trial has reached full enrollment with 65 treated patients.
Specialty Devices > Cardiovascular Devices > News
Philips to acquire EPD Solutions for EUR250m
By MDBR Staff Writer
Royal Philips has agreed to acquire EPD Solutions, a member of the Hobart Group companies, for an upfront cash consideration of €250m.
Specialty Devices > Cardiovascular Devices > News
TRiCares secures funding for transcatheter-based tricuspid valve replacement system
By MDBR Staff Writer
French medical device start-up firm TRiCares has secured €22m funding to advance the development of its transcatheter-based tricuspid valve replacement system.
Specialty Devices > Cardiovascular Devices > News
Ancora Heart raises $17.8m funding for heart failure therapy
By MDBR Staff Writer
US-based Ancora Heart has raised $17.8m financingto support continued clinical assessment of its AccuCinch ventricular repair system.
Specialty Devices > Cardiovascular Devices > News
Study shows RenalGuard-guided diuretic therapy improves breathing patterns in ADHF patients
By MDBR Staff Writer
RenalGuard Solutions’ clinical trial showed that RenalGuard-guided diuretic therapy has improved breathing patterns and diuretic efficiency in acute decompensated heart failure (ADHF) patients.
Specialty Devices > Cardiovascular Devices > News
Getinge reports positive trends for IABP therapy in SEMPER FI pilot study
By MDBR Staff Writer
Getinge said that its intra-aortic balloon pump (IABP) has shown positive results in a pilot study evaluating the balloon therapy for patients with extensive myocardial infarction (MI or heart attack).
Specialty Devices > Cardiovascular Devices > News
FDA recalls Abbott’s HeartMate 3 due to potential malfunction
By MDBR Staff Writer
The US Food and Drug Administration (FDA) has issued a Class I Recall of Abbott’s HeartMate 3 Left Ventricular Assist System, because of potential malfunction that may lead to graft occlusion.
Specialty Devices > Cardiovascular Devices > News
QT Vascular to divest coronary assets to Teleflex
By MDBR Staff Writer
Singapore-based firm QT Vascular has signed an asset purchase and option agreement (APOA) with US-based Teleflex Life Sciences Unlimited Company and Teleflex for the sale of its intellectual property rights to its non-drug coated coronary products, including Chocolate XD and Glider.
Specialty Devices > Cardiovascular Devices > News
Ultromics secures funding for AI heart diagnostic technology
By MDBR Staff Writer
UK start-up Ultromics has secured £10m funding to advance the commercialization of artificial intelligence (AI) technology for the diagnosis of coronary heart disease.
Specialty Devices > Cardiovascular Devices > News
1-15 of 2980 results