April 26, 2010 – A vascular closure device using a single suture fitted with stainless steel rings was recently cleared by the U.S. Food and Drug Administration (FDA)

April 19, 2010 — The latest research in a series of studies at The Children’s Hospital of Philadelphia demonstrate the feasibility of magnetically guided nanoparticles as a new delivery platform for a variety of possible therapeutic cargos, including DNA, cells and drugs. The novel technique achieved better results at a lower dose than conventional non-magnetic stent therapy.

April 21, 2010 — A landmark clinical trial has begun in Europe to explore the safety and efficacy of a paclitaxel-eluting stent for the treatment of renal artery disease.

April 23, 2010 - Vendor-neutral picture archive and communication systems (PACS) are facilitating interoperability across existing modalities and networks.

April 22, 2010 – Broadening its product scope into the peripheral artery disease market, Medtronic today received U.S. Food and Drug Administration (FDA) clearance for the Complete SE Vascular Stent System. The self-expanding stent is indicated for used for the treatment of peripheral arterial disease (PAD) in the iliac arteries.

April 22, 2010 – Instead of using a conventional spring coil design, a new guidewire uses a micro-cut nitinol sleeve for improved torque control. The Kinetix Guidewire was launched today for use in percutaneous coronary intervention (PCI) procedures.

April 22, 2010 - With the proliferation of telemedicine and tereradiology services, the two fields are crossing paths on over health care networks, and in particular in image-enabled electronic health records (EHRs), also known as image exchanges.

April 22, 2010 – Two new electrocardiogram (ECG) devices released this week aid workflow in high-volume hospital departments. Spacelabs Healthcare began the global market release its CardioExpress, SL12 and SL6 resting ECG units.

April 21, 2010 – A stent that captures endothelial progenitor cells is now combined with thin cobalt chromium stent struts with a low profile for greater flexibility and deliverability. The Genous Bio-Engineered Cobalt Chromium Stent recently received CE mark approval for commercial release in Europe.

April 21, 2010 – A second generation, force-sensing ablation catheter released this week in Europe, gives physicians a real-time, objective measure of contact force during the treatment of cardiac arrhythmias. It includes a smaller fiber optic sensor at the tip, a force-time integral display and automatically generated summary reports of the procedure.

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