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January 27, 2012 โ€” Crux Biomedical announced it received CE mark approval for its inferior vena cava filter (IVCF) with bi-directional retrieval (BDR). Vena cava filters are designed to trap blood clots that can lead to a potentially fatal pulmonary embolism (PE). Each year in the United States, approximately 600,000 patients develop a PE and an estimated 200,000 deaths occur.

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January 27, 2012 โ€” Arizona Heart has chosen Ziehm digital flat-panel C-arms for its three advanced technology suites. The Ziehm Vision RFD hybrid edition delivers distortion-free, high-resolution images for interventional procedures, and represents a cost-efficient alternative solution to fixed installed systems.

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January 26, 2012 โ€” Heart Hospital of Austin opened a heart valve clinic, the first of its kind in the region. The clinic gives new hope to patients with severe aortic stenosis who were previously considered inoperable, offering a multidisciplinary approach to evaluating such cases.

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January 26, 2012 โ€” The RhinoChill IntraNasal cooling system has been nominated for one of the European medical device industryโ€™s most prestigious awards.

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January 26, 2012 โ€” Amorcyte LLC, a NeoStem company, announced the enrollment of the first patient in the Amorcyte PreSERVE Phase II trial for acute myocardial infarction. The study is a multicenter, randomized, double-blind, placebo-controlled clinical trial to evaluate the safety and efficacy of infarct-related artery infusion of AMR-001, an autologous bone marrow derived cell therapy enriched for CD34+ cells.

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Technology

January 25, 2012 โ€” CJPS Medical Systems announced that VitalPoint, its remote patient monitor, can be used with Microsoft Windows-based tablet PCs. This announcement comes on the heels of CJPS being the first company to waive all connectivity fees to caregivers accessing their patients' data remotely using home monitors.

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January 25, 2012 โ€” Which Medical Device announced the winner of its Device of the Year Award 2011 in the cardiology category.

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January 25, 2012 โ€” CardioFocus, Inc. developer of the HeartLight Endoscopic Ablation System (EAS) for the treatment of atrial fibrillation (AF) announced that a new study in the Journal of Cardiovascular Electrophysiology demonstrated the high acute and chronic success rates achievable with a single AF ablation procedure using HeartLight EAS.

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January 25, 2012 โ€” Terumo Cardiovascular Systems announced today that it has entered into an exclusive agreement with LAAx Inc. to distribute the TigerPaw System II, a left atrial appendage (LAA) closure device in the United States.

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January 25, 2012 โ€” Physicians at University Hospitals (UH) Case Medical Center enrolled their first patient in LEVANT 2, a global, multicenter, randomized clinical trial evaluating the safety and efficacy of the Moxy drug-coated balloon for the treatment of peripheral arterial disease (PAD).

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Technology

January 25, 2012 โ€” Rhode Island Hospital is the first hospital in the world to acquire the BodyTom portable, intra-operative, multi-slice computed tomography (CT) body scanner.

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January 25, 2012 โ€” Philips Healthcare announced the release of the Xper Flex Cardio Physiomonitoring system, a hemodynamic cardiac monitoring solution used to facilitate invasive investigation of heart and vascular disease.

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January 23, 2012 โ€“ Boston Scientific Corp. said the U.S. District Court for the District of New Jersey has found all the asserted patents for a coronary stent in a lawsuit brought by Johnson & Johnson to be invalid and entered judgment in favor of Boston Scientific.

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Feature | Dave Fornell

The next big advancement in cardiac imaging is likely to be computed tomography (CT) perfusion imaging. This enables one commonly available modality to image both the detailed anatomy and function of the heart at the same time. The impact on medicine could reduce healthcare costs by eliminating some hospital stays, cutting the number of tests and speeding patient diagnosis.

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Technology

January 23, 2012 โ€” CardioComm Solutions, Inc. a provider of ECG acquisition and management software solutions, received clearance from the U.S. Food and Drug Administration (FDA) for over-the-counter (OTC) sales and marketing of their consumer-based, hand-held heart rhythm monitor known as the HeartCheck Pen Handheld ECG.

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