July 9, 2009 – According to Millennium Research Group (MRG), the ongoing economic crisis is putting pressure on publicly funded European healthcare systems, intensifying the decline of interventional cardiology device prices in the region.
SunTech Medical offers clinical-grade blood pressure technology in the form of its OEM Non-invasive Blood Pressure module. This technology is included in ExpressMD's Electronic House Call remote patient monitoring device for telemedicine. As a feature of the house call device, the module provides professional grade BP monitoring to allow easy in-home use.
July 9, 2009 – SunTech Medical said today its clinical-grade blood pressure technology will be included in ExpressMD’s Electronic House Call remote patient monitoring device for telemedicine.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
July 9, 2009 – Coherex Medical Inc. today said its Coherex FlatStent EF PFO Closure System has been granted CE mark clearance for use in Europe and other countries to close patent foramen ovales (PFOs), a common heart defect found in approximately 20 percent of the worldwide population.
July 9, 2009 –Stentys said today it received CE mark approval for the European sale of its disconnectable and self-expanding stent platform for treatment of coronary artery bifurcations.
July 9, 2009 - Volcano Corporation said yesterday it signed a termination agreement with its largest distributor in Japan, Goodman Company Ltd., enabling Volcano to accelerate its transition to a direct sales force in the market to support its intravascular ultrasound (IVUS) and functional measurement (FM) consoles and disposables.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
July 9. 2009 - Vascular Solutions, Inc. announces the availability of the new Trespass angiographic catheter specifically designed for use by interventional radiologists and other physicians performing endovascular Abdominal Aortic Aneurysm (AAA) repair procedures.
July 9, 2009 - The U.S.
July 8, 2009 – Bioheart Inc. said this week a panel discussion on myoblast (muscle stem cell) therapy between distinguished physicians gave the technology a big endorsement.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
July 8, 2009 - Pluristem Therapeutics Inc. said yesterday its first patient enrolled in a phase I clinical trial that will evaluate the safety of the company’s allogeneic, placental-derived, adherent stromal cell product, termed PLX-PAD. The product is for use in patients afflicted with critical limb ischemia (CLI), the end-stage of peripheral artery disease (PAD).
July 8, 2009 – CardioFocus Inc. said yesterday it received a CE mark in Europe for its Endoscopic Ablation System (EAS) to treat patients with atrial fibrillation.
July 8, 2009 - Marc Gerdisch, M.D., director of cardiothoracic surgery at the St. Francis Heart Center and a partner at Cardiac Surgery Associates, is using the CorMatrix Extracellular Matrix (ECM) to modify and repair cardiac structures, allowing heart tissue to regrow inside the beating hearts of heart surgery patients.
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
July 8, 2009 – A procedure that sends targeted energy into the heart through a catheter can be used to treat a common type of irregular heartbeat, but little is known about the treatment's long-term benefits and the best methods and circumstances for applying it, according to a new report funded by the Health and Human Services' (HHS’) Agency for Healthcare Research and Quality (AHRQ).
July 8, 2009 - Covidien said today Health Canada approved the company’s abbreviated new drug submission (ANDS) for its kit for the preparation of technetium Tc 99m Sestamibi injection. Covidien’s generic product is fully substitutable for Cardiolite, the company said.
July 8, 2009 - Ziosoft Inc., a leader in advanced visualization and analysis software for medical imaging, has received 510(k) clearance from the United States Food and Drug Administration (FDA) to market its magnetic resonance (MR) cardiac function analysis application for use with the Ziostation thin-client system.