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Brand Castle Recalls Limited Quantities of in The Mix Monkey Bread Mix Due to Possible Salmonella Contamination
Dec 13, 2016Brand Castle is voluntarily recalling limited quantities of our In the Mix Monkey Bread Mix because it has the potential to be contaminated with Salmonella. This product is being recalled because an ingredient supplier (Valley Milk ...
Tags: Brand Castle, Salmonella
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Covidien Has Purchased a Small California Medtech Company
Aug 26, 2014As it prepares for its $43 billion merger with Medtronic, Covidien has purchased a small California medtech company. The price was not disclosed. Privately held Reverse Medical Corp. (Irvine, CA) makes devices to manage acute stroke and ...
Tags: Covidien, Medtech Company, Health
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Cancer Death Rates Continue to Decline in The United States
Dec 26, 2013Cancer death rates continue to decline in the United States, mainly because anti-smoking efforts have caused a drop in lung cancer deaths, researchers report. From 2001 through 2010, death rates for all cancers combined decreased by 1.8 ...
Tags: cancer death rates, US, anti-smoking efforts
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Bolton Medical Has Initiated Its Phase II Us Clinical Trial
Dec 6, 2013Bolton Medical, a medical device manufacturer, has initiated its Phase II US clinical trial to study the safety and effectiveness of the Treovance abdominal stent-graft with Navitel delivery system. The first two cases were performed on ...
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The FDA Granted The Direxion a 510(k) Clearance
Nov 26, 2013The Direxion Torqueable Microcatheter-a microcatheter for shrinking tumors or blocking aneurysms-has won FDA and CE Mark approval, Boston Scientific recently announced. The FDA granted the Direxion a 510(k) clearance because it retains ...
Tags: Boston Scientific Microcatheter, FDA Approval, Direxion a 510(k)
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Israeli Device Manufacturer ITGI Medical Announced a Partnership with Vascular Solutions
Nov 22, 2013Israeli device manufacturer ITGI Medical announced a new partnership with Vascular Solutions. Under the new agreement, both companies will work together to land a Humanitarian Device Exemption (HDE) from FDA regulators for the ITGI ...
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Medtronic Branch Thoracic Stent Graft System Demonstrated Proof of Concept
Nov 22, 2013Medtronic's Valiant 'Mona LSA' branch thoracic stent graft system demonstrated proof of concept in a first-in-human study being conducted under the US Food and Drug Administration (FDA)'s ‘Innovation Pathway’ early feasibility ...
Tags: stent graft system, Medicine
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Fried Foods Damage Your Body and Brain in Many Different Ways
Nov 19, 2013Fried foods damage your body and brain in many different ways, and it's not just a long term consequence, but a short term detriment as well. Just as a car needs good clean oil to run efficiently and not break down, your body needs food ...
Tags: Fried Foods, Agriculture, Food
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Gore Announces Dr Brian in Gore Excluder Iliac Branch Study
Nov 18, 2013W. L. Gore & Associates (Gore) has announced that Dr Brian Peterson from Saint Louis University, enrolled the first patient in the Gore EXCLUDER iliac branch clinical study. The clinical study is a prospective, multi-center, ...
Tags: Medicine, Gore Excluder
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ITGI Medical Has Signed a Strategic Cooperation Agreement with Vascular Solutions
Nov 14, 2013Israeli bio-medical engineering company ITGI Medical has signed a strategic cooperation agreement with Vascular Solutions, a medical device company, to commercialize ITGI's Aneugraft Dx coronary covered stent in the US market. Pursuant to ...
Tags: ITGI Medical, Aneugraft DX Stent
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CE Mark Approva Will Be Obtained by Gore for Its Gore Excluder Iliac Branch Endoprosthesis
Nov 12, 2013W. L. Gore & Associates (Gore) has obtained CE Mark approval for its GORE EXCLUDER iliac branch endoprosthesis, designed for the endovascular treatment of common iliac artery aneurysms or aortoiliac aneurysms. Gore has designed the iliac ...
Tags: CE, Gore, GORE EXCLUDER, product line
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Pulsar Vascular Has Obtained CE Mark Approval for Its Pulserider Device
Oct 17, 2013US-based Pulsar Vascular has obtained CE Mark approval for its PulseRider device, designed to bridge the neck of cerebral aneurysms previously not amenable to endovascular therapy. With this CE Mark approval, the company now has full ...
Tags: Pulsar Vascular, CE Mark Approval
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Lombard Medical Treated The First Us Patients with Aorfix
Aug 29, 2013Medical technology company Lombard Medical Technologies successfully treated the first US patients with Aorfix, its flexible stent graft for the endovascular repair of abdominal aortic aneurysms (AAAs). Meriter Hospital vascular surgeon ...
Tags: Aortic Stent Graft
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Trivascular Has Commenced The US PAS of The Abdominal Stent Graft System for AAA
Jul 19, 2013US medical device company TriVascular has commenced the US Post-Approval Study (PAS) of the Ovation Prime Abdominal Stent Graft System for the treatment of abdominal aortic aneurysms (AAA). The Ovation System and the Ovation Prime System ...
Tags: TriVascular, medical device
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a New Method for The Diagnosis of Retinal Microaneurysm Was Ethan Launched
Jun 13, 2013The Hebrew University of Jerusalem’s Yissum Research Development Company has developed a novel method to diagnose retinal micro-aneurysms that pose a high risk for leakage, a primary cause of diabetic retinopathy. The novel method ...
Tags: Yissum, Retinal Micro-Aneurysms
