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NOTICIAS


03 junio 2012

Gore® Hybrid Vascular Graft Honored as Gold Winner in the 2012 Medical Design Excellence Awards

BioSpace. BUSINESS WIRE

W. L. Gore & Associates (Gore) today announced that the GORE® Hybrid Vascular Graft was awarded Gold Winner in the Implant and Tissue-Replacement Products category of the 2012 Medical Design Excellence Awards (MDEA) competition. The Gore Device is an expanded polytetrafluoroethylene (ePTFE) vascular prosthesis that provides a streamlined solution for challenging dialysis access, aortic debranching, and arterial bypass procedures. The award-winning prosthesis provides a new way in for better outflow and the potential to significantly improve patient outcomes.

29 mayo 2012

MAQUET Cardiovascular Announces Acquisition of the Avalon Elite(R) Bi-Caval Dual Lumen Catheter and Complimentary Vascular Access Kits from Avalon Laboratories

Healthcare Sales & Marketing Network.

MAQUET Cardiopulmonary, a business unit of MAQUET Cardiovascular and a leader in extracorporeal life support (ECLS) systems, today announced that they have signed an agreement with Avalon Laboratories to acquire its Avalon Elite® Bi-Caval Dual Lumen Catheter and complimentary vascular access kits for use during ECLS.

15 noviembre 2011

Cotavance drug-eluting balloon reduced five-year target lesion revascularisation rates by 59% in PAD patients

Interventional NEWS

Five-year data from the THU"DER trial demonstrated a 59% relative reduction in target lesion revascularisation rates in popliteal arteries of patients with peripheral arterial disease (PAD) treated with the Cotavance drug-eluting balloon (Medrad) with Paccocath technology compared to standard balloon angioplasty. Additionally, for patients requiring target lesion revascularisation, the average time to revascularisation before target lesion revascularisation was extended by 448 days in patients treated with the Cotavance catheter.

16 septiembre 2014

Initial data from real-world IN.PACT Admiral drug-coated balloon registry show 8.7% reintervention rate at one year

Vascular News

Initial data from the IN.PACT Global study, presented at the 2014 Transcatheter Cardiovascular Therapeutics (TCT) conference (Washington, DC, USA) show a clinically-driven target lesion revascularisation rate of 8.7% at 12 months for the first 655 patients enrolled in the study. According to Medtronic, the data validate the findings from the IN.PACT SFA trial.

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