May 28, 2009 - Boston Scientific Corp. said yesterday it received FDA clearance to market its TAXUS Liberte Atom Paclitaxel-Eluting Coronary Stent System, a next-generation drug-eluting stent (DES) specifically designed for treating small coronary vessels.
May 28, 2009 – Lantheus Medical Imaging Inc. today said it completed patient enrollment of CaRES (Contrast Echocardiography REgistry for Safety Surveillance), the first, multicenter phase IV observational registry that evaluates the use of ultrasound imaging agents in routine clinical practice.
May 26, 2009 – HeartCare Cardiovascular Specialists in Libertyville, Ill. expanded its CVIS capabilities with a new DigiNet Pro system. This system will provide the site with Web access enabling users to have full CVIS capability from anywhere at anytime.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
May 26, 2009 - ProSolv Cardiovascular, a Fujifilm company, this week released its Synapse ProSolv Cardiovascular version 4.0.2 software.
May 27, 2009 - Cytori completed enrollment in the first study to investigate adipose derived stem and regenerative cells in chronic heart disease.
May 26, 2009 – The Medical Imaging and Technology Alliance said today a recent study conducted by researchers at the University of Pennsylvania confirms computed tomography angiography (CTA) to be a safe, effective and cost-efficient means of ruling out cardiovascular disease in patients presenting to the emergency room with chest pain. The results of this landmark study were presented at the
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
Medical Education Technologies (METI) offers its Human Patient Simulators for medical education programs, allowing learners to develop a high level of confidence and, ultimately, a demonstration of competence.
The virtual-reality CathLabVR System by Immersion Medical fills roughly the same space as real cath lab equipment. It includes two monitors. One displays fluoroscopic views, virtual assistant functions, navigation control, and simulated patient information. The other is for displaying physio, cine, and still images.
The new and enhanced VIST Enhanced Carotid and Coronary 7.7 training modules feature vital signs, complications, medication management and measurement functionality enhance to create clinical realism and elevate the educational value of simulation training. The system includes new patient cases, including chronic total occlusion and transradial access.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
May 26, 2009 – AMG International GmbH last week submitted its second-generation drug-eluting stent (DES), Itrix, for regulatory review in Europe. The stent offers a bioabsorbable polymer that holds the drug.
May 26, 2009 – Biotronik Inc. recently launched its Lumax 540 series implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillator (CRT-D) devices during Heart Rhythm 2009.
May 26, 2009 – Medtronic intends to seek FDA approval for the use of cardiac resynchronization therapy (CRT) in certain mildly symptomatic heart failure patients. While CRT is a proven life-saving therapy for some patients with advanced stages of heart failure (New York Heart Association Class III, IV), it is not currently approved for use in earlier stages, or mildly symptomatic patients.
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
May 26, 2009 - United Therapeutics Corp. said today the FDA approved ADCIRCA (tadalafil) tablets for oral administration, with a recommended dose of 40 mg, as the first once-daily phosphodiesterase type 5 (PDE5) inhibitor for the treatment of pulmonary arterial hypertension (PAH).
May 22, 2009 - Rafael Medical Technologies Inc. said this week it received FDA clearance for its SafeFlo Vena Cava Filter. The clearance is for the permanent implantation of the filter in patients at risk of pulmonary embolism. CE mark was granted for the filter in 2004 for both permanent and retrieval indications.
May 22, 2009 - CPC of America Inc. filed its first patent of a synthetic sealant for the MedClose Vascular Closure System (VCS), which is an internal puncture-closing system for use in percutaneous intravascular diagnostic and interventional procedures.