Technology
July 10, 2009 – Spectranetics Corp. said today it received FDA-clearance to market the Turbo-Tandem, a single-use, disposable device indicated for atherectomy of infrainguinal arteries. CE mark approval is also in place for marketing within the European Union and was received earlier this month.
July 10, 2009
News
July 9, 2009 – The 30-day mortality and readmission rates for acute care of heart attack and heart failure patients vary significantly from hospital to hospital across the nation, according to a new study published in a current issue of Circulation, the journal of the American Heart Association.
July 09, 2009
News
July 9, 2009 – Sorin Group said this week Health Canada cleared the REPLY family of dual- and single-chamber rate adaptive pacemakers.
July 09, 2009Sponsored Content
Feature | Information Technology
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
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July 9, 2009 – InTouch Health today released Multi-Presence, a new software that expands the company’s remote presence telehealth offering, enabling multiple physicians at different locations to simultaneously access the same consultation for collaboration on patient care anywhere.
July 09, 2009News
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.
July 09, 2009Technology
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 09, 2009Sponsored Content
Feature | Cardiac Imaging
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
March 05, 2024Technology
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.
July 09, 2009
News
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 09, 2009
News
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 09, 2009Sponsored Content
Blog
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
December 11, 2023
News
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.
July 09, 2009
Technology
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 09, 2009
News
July 9, 2009 - The U.S.
July 08, 2009Sponsored Content
Case Study | Hemodynamic Monitoring Systems
Change Healthcare Cardiology Hemodynamics is an integrated hemodynamic monitoring system for monitoring vital signs and ...
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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.
July 08, 2009News
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 08, 2009News
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.
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