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NOTICIAS


31 diciembre 2012

Paired CT Scans Catch Chemo-Killing of Liver Tumors in Real Time

Science Daily

Using two successive pairs of specialized CT scans, a team of Johns Hopkins and Dutch radiologists has produced real-time images of liver tumors dying from direct injection of anticancer drugs into the tumors and their surrounding blood vessels. Within a minute, the images showed whether the targeted chemotherapy did or did not choke off the tumors blood supply and saved patients a month of worry about whether the treatment, known as chemoembolization, was working or not, and whether repeat or more powerful treatments were needed.

23 enero 2013

Associations Look to Magazines to Enhance Membership Experience

Audience

In an effort to better serve their members, two associations are jumping into the magazine publishing business—the Society of Interventional Radiology (SIR) and the National Association of Home Builders (NAHB) have each launched new magazines to better communicate critical information and industry updates to their core groups.

EDAP Submits U.S. FDA Pre-Market Approval Application for Ablatherm(R)-HIFU for Treatment of Low Risk, Localized Prostate Cancer

20130202

EDAP TMS SA (EDAP), the global leader in therapeutic ultrasound, announced today the submission of its Pre-Market Approval (PMA) application to the U.S. Food and Drug Administration (FDA) on January 31, 2013 for the Company s Ablatherm-HIFU (High Intensity Focused Ultrasound) for treatment of low risk, localized prostate cancer. EDAP s PMA submission includes data from the ENLIGHT study, a multi-center U.S. Phase II/III clinical trial that completed the two year follow-up needed to evaluate its primary endpoint in August 2012, as well as data from the Company s extensive worldwide database of treatment information and follow-up data from patients who have undergone HIFU therapy for prostate cancer

14 enero 2013

Indian stent makers target international markets

Fierce Medical Devices

Indian stent makers are becoming increasingly viable competitors in international markets, adding another layer to an industry already crowded with a number of players.

14 enero 2013

Blockade MedicalTM Announces First 100 Patients Treated with the Barricade Coil System

Device Space

IRVINE, Calif.--(BUSINESS WIRE)--Blockade Medical LLC, a privately held company focused on the development of catheter based therapeutic devices for the treatment of cerebral aneurysms, announced today that more than 100 patients have been successfully treated with the Barricade Coil SystemTM. The patients treated, presented with a wide range of cerebral aneurysms and peripheral lesions. All treated patients had positive clinical outcomes without any reported complications.

09 enero 2012

FDA Clears Software That Helps Radiologists Rapidly and Accurately Confirm Placement of Lifesaving Medical Devices

The Healthcare Sales & Marketing

DAYTON, Ohio--(Healthcare Sales & Marketing Network)--ClearRead +Confirm, new software from Riverain Technologies that improves the clarity of conventional chest X-ray images and allows radiologists to rapidly confirm the proper placement of tubes, lines and wires, has received 510(k) clearance from the Food and Drug Administration (FDA).

19 diciembre 2012

One-year results from the Symplicity HTN-2 show sustained reduction in blood pressure with the Symplicity renal denervation system

Interventional NEWS

Results from the Symplicity HTN-2, the first randomised clinical trial investigating renal denervation, were published online before print in Circulation, the Journal of the American Heart Association. These data showed patients, who initially received treatment with the Symplicity renal denervation system (n=47), sustained a significant drop in blood pressure (-28/-10 mm Hg [p<0.001]) compared to baseline at 12 months. The 12 month results demonstrated preservation of the benefit at six month follow-up (-32/-12 mm Hg). No device related serious adverse events, no late vascular complications, and no significant decline in kidney function were reported at 12 months.

11 diciembre 2012

Upgraded version of Accu2i pMTA microwave ablation device gets FDA clearance

Interventional NEWS

The initial version of the single, high-power, high-frequency 2.45GHz saline-cooled needle was cleared for use in the USA as part of the Acculis MTA system in 2010. Following two years of global distribution, and in response to customer feedback and growing product demand, Microsulis has updated the device’s design and manufacturing process. Improvements include a refined optically clear moulded handle and improved connection cartridge.

06 diciembre 2012

WallFlex Biliary RX Fully Covered Stent study enrols first patient

Interventional NEWS

Boston Scientific has announced that the first patient has been enrolled in a study comparing its WallFlex Biliary RX Fully Covered self-expanding metal stent (SEMS) to plastic stents for the treatment of benign bile duct strictures caused by chronic pancreatitis.

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