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NOTICIAS


20 febrero 2013

OrbusNeich Files Patent Infringement Actions Against Boston Scientific in Germany and the Netherlands

Healthcare Sales & Marketing Network

OrbusNeich today announced that OrbusNeich Medical GmbH and Orbus International B.V., subsidiaries of OrbusNeich Medical, Inc., (collectively, "OrbusNeich") have commenced patent infringement actions in Germany and The Netherlands against Boston Scientific Corporation (BSX) ("Boston Scientific") and its distribution affiliates in those countries

13 febrero 2013

Loma Vista Medical Reports That It is Ramping up Sales in U.S. and Europe of its FDA-Cleared and CE-Marked TRUE Dilatation(TM) Balloon Valvuloplasty Catheter Specifically Designed to Reduce Rapid Pacing Time and Prevent Balloon Failure

Healthcare Sales & Marketing Network

Loma Vista Medical has established a direct sales force within the United States and a network of seven European distributors working to commercialize the world’s first ultra-precise balloon catheter specifically designed to meet the demands of transcatheter valve procedures.

18 enero 2013

St. Jude Medical (STJ) Receives CE Mark of Next-Generation Cardiac Device for Stroke Prevention

Device Space

ST. PAUL, Minn.--(BUSINESS WIRE)-- St. Jude Medical, Inc. (STJ), a global medical device company, today announced European CE Mark approval of its AMPLATZER™ Amulet™ Left Atrial Appendage Occluder. The Amulet device is used to close the left atrial appendage (LAA) in patients diagnosed with non-valvular atrial fibrillation (AF). According to research, AF leads to an increased risk for stroke. Sealing off the LAA helps prevent the risk of blood clot formation and release, potentially reducing the risk of stroke. The next-generation percutaneous transcatheter device leverages the design and clinical success of the original AMPLATZER™ Cardiac Plug with additional features allowing treatment of a wider range of appendage anatomies. St. Jude Medical will be showcasing the new AMPLATZER Amulet device during the eighteenth annual Boston AF Symposium at booth 319.

17 enero 2013

FDA Clears Sanovas Vas Zeppelin Smart Catheter for Lung Cancer

Device Space

SAUSALITO, Calif., Jan. 17, 2013 /PRNewswire/ -- Sanovas Inc., a life science technology company developing and commercializing the next-generation of micro-invasive diagnostics, devices and drug delivery technologies, announced today that it has filed with the U.S. Food and Drug Administration for clearance of the company s Vas Zeppelin Smart Catheter for the treatment of chronic pulmonary diseases and lung cancer. The technology would be among the smallest interventional catheters commercially available, allowing physicians to access and deliver therapy to some of the tiniest and most remote passageways in the anatomy.

17 enero 2013

Se presenta iVascular ante 400 profesionales del sector médico en la Galería de Cristal del Palacio Cibeles de Madrid.

Noticias Médicas

Madrid, Enero de 2013.- El pasado jueves 10 de enero iVascular celebró su evento de presentación en Madrid. La Galería de Cristal del Palacio Cibeles acogió a los 400 profesionales del sector médico que acudieron a la cita para conocer el proyecto iVascular, una empresa enfocada al diseño y fabricación de dispositivos e implantes en el área cardiovascular, con alto componente tecnológico e innovador.

14 enero 2013

Stent firms find pulse overseas too

Daily News & Analysis

After drugmakers, it is the turn of stent manufacturers to explore markets overseas. South East Asia, Middle East, Latin America, Eastern Europe — regions where regulatory clearances are relatively easy to get — are particularly attractive for these players.

14 enero 2013

Phoenix Cardiac Devices announces start of clinical trial in India and Europe to test BACE(TM) device for treatment of mitral regurgitation without open heart surgery

The Healthcare Sales & Marketing

CHICAGO, Jan. 14, 2013 -- (Healthcare Sales & Marketing Network) -- Phoenix Cardiac Devices, Inc., a medical device company with a novel method of repairing leaky heart valves without open-heart surgery, has enrolled its first patient in a clinical trial aimed at achieving CE Mark approval in Europe.

11 enero 2013

Nace iVascular, un proyecto español innovador que apuesta por la integración tecnológica para desarrollar terapias y dispositivos avanzados para el sistema cardiovascular

Noticias Médicas

Madrid, enero de 2013.- Life Vascular Devices, Polytech, Cardiva, Kern Pharma, y Ames; empresas todas ellas de referencia en sus sectores de actividad, han unido sus recursos y know-how para crear la compañía iVascular, dedicada al diseño y fabricación de dispositivos e implantes en el área cardiovascular, con alto componente tecnológico e innovador.

09 enero 2013

Abbott commences massive dissolving stent trial in U.S.

Fierce Medical Devices

Abbott ($ABT) this week launched a massive U.S. clinical trial for its Absorb drug-eluting bioresorbable vascular scaffold, with plans to enroll up to 2,250 patients. If the results pass muster, they ll support the company s FDA approval bid.

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