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February 9, 2012 — The U.S. Food and Drug Administration (FDA) sent a warning letter to Merit Medical Systems Inc. regarding modifications to the hydrophilic coating process for the Merit Laureate Hydrophilic Guidewire, following an inspection of the company's facility in Galway, Ireland.

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February 9, 2012 — Stereotaxis Inc. said its Vdrive robotic navigation system, which provides physicians the ability to remotely manipulate traditionally non-robotic catheters, is growing in popularity and is expected to surpass 500 clinical procedures in Europe in February.

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Technology

February 9, 2012 — Boston Scientific announced the United States launch of the TruePath CTO device, designed to facilitate the crossing of chronic total occlusions (CTOs, or complete blockages) within the peripheral vasculature.

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St. Jude Medical has launched its Unify Quadra cardiac resynchronization therapy defibrillator (CRT-D) and Quartet left ventricular quadripolar pacing lead. It features four electrodes spaced over 4.7 cm, enabling up to 10 pacing configurations for better cardiac rhythm management.

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February 9, 2012 — Healthcare imaging specialist Barco announced that it has signed an agreement to acquire U.K.-based JAOtech, a manufacturer of patient entertainment and point-of-care terminals for hospitals.

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February 9, 2012 — Valley Presbyterian Hospital (VPH) was the site for the first implantation in the United States of a new heart device since the U.S. Food and Drug Administration (FDA) approved the DF4 High-Voltage Connector System by Medtronic earlier this month, Gus Valdespino, VPH president and CEO announced.

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February 9, 2012 — DSM announced a successful collaboration with medical manufacturer EPflex Feinwerktechnik GmbH to launch a new set of guidewires with ComfortCoat hydrophilic coating, a proprietary DSM technology.

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February 9, 2012 — Wolters Kluwer Health announced King’s Daughters Medical Center has selected its ProVation MD software for cardiology procedure documentation and coding in its cardiac catheterization labs.

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A 3-D view does more than make for exciting movies in a theater; it can also improve the care of animals. The Chicago Zoological Society’s (CZS) Brookfield Zoo is the first North American zoo to use revolutionary 3-D imaging technology with on-site digital radiology and computed tomography (CT) equipment in its state-of-the-art animal hospital. The new technology allows the Society’s veterinarians to enhance two-dimensional CT scans, MRIs and ultrasounds with 3-D models that will enable them to better treat zoo animals.

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February 6, 2012 — InspireMD Inc. announced positive clinical results for its MGuard stent from a controlled randomized trial conducted in Chile.

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February 6, 2012 — A medical technology company commercializing the world's first and only self-apposing stent to treat acute myocardial infarction (AMI), announced today that the APPOSITION III clinical study successfully enrolled 1,000 patients suffering from a severe heart attack and that the final results of the examination 30 days after treatment will be presented during the upcoming EuroPCR international cardiology congress.

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February 6, 2012 — Vascular Solutions Inc. announced it is marketing a reprocessing service for the ClosureFAST radiofrequency ablation catheter in the United States

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February 6, 2012 — GE Healthcare recently announced a long-term agreement with Biosense Webster Inc. in which the companies will co-distribute their leading electrophysiology (EP) systems.

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February 3, 2012 – The U.S. Food and Drug Administration (FDA) approved the premarket approval application (PMA) for the St. Jude Medical Therapy Cool Path Duo and Satire BLU Duo ablation catheters and the IBI 1500T-9 VI.6 cardiac ablation generator.

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February 3, 2012 — Colibri Heart Valve received an notification it received patents for a new transcatheter heart valve from the United States Patent and Trademark Office.

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