Technology

Sony Electronics announced the world's first medical-grade monitor, model PVM-2551MD, based on organic light-emitt...

The 3-D medical-grade 32-inch class monitor, the EJ-MDA32U-K, from Panasonic, is fully compliant with medical equipment standards, delivers exceptional 2-D and 3-D image quality, and can display mu...

TriReme Medical Inc. (TMI) announced that it has received U.S....

Angioslide Ltd., a provider of embolic capture angioplasty solutions, today announced the successful deployment of a 3x100 mm Proteus device for treating peripheral artery disease (PAD) in bel...

Ultrasonix Medical Corporation has received approval from the U.S. Food and Drug Administration (FDA) for its SonixGPS technology for vascular access procedures.

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St. Jude Medical received 510(k) clearance from the U.S....

r4 Vascular Inc. received clearance in July 2012 from the U.S....

As the largest diameter rotational atherectomy device in the Jetstream catheter family, the Jetsream Navitus L atherectomy catheter can create a lumen 30 percent larger than the standard Navitus de...

Bayer HealthCare’s Radiology and Interventional unit has launched the new Mark 7 Arterion Injection System, the latest in the Medrad Mark series of angiographic injectors.

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TriReme Medical Inc. received U.S....

Surefire Medical's Surefire high-flow microcatheter is the next generation of the company's infusion technology....

Cardiosolutions Inc.'s Dexterity Steerable Introducer, a next-generation structural heart access introducer and delivery conduit, received 510(k) clearance from the U.S....

Medtronic Inc. launched the Endurant II AAA Stent Graft System in the United States in June 2012 following approval from the U.S....

The Hansen Medical Magellan Robotic System is the first robotic navigation system to more precisely guide 

The 32 and 38 mm lengths of Boston Scientific's Promus Element Plus everolimus-eluting platinum chromium (PtCr) coronary stent system, the company's next-generation

TriReme Medical Inc. announced on May 23, 2012, approval by the U.S....

Boston Scientific's Epic Vascular Self-Expanding Stent System is designed to open blocked arteries in patients with iliac artery stenosis, a form of 

Maquet Cardiovascular LLC announced it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its new Mega 7.5 Fr....

In May 2012 GE Healthcare introduced a new version of its Vscan pocket-sized visualization tool, developed to deliver imaging capabilities at the point of care....

Angioslide Ltd., a provider of embolic capture angioplasty solutions, announced in May 2012 that it received FDA 510(k) clearance for its new 3x100 mm Proteus device for treating peripheral artery ...

The U.S. Food and Drug Administration (FDA) has approved the premarket approval application (PMA) for the Medinol Ltd....