As with other Cordis Endovascular percutaneous transluminal angioplasty (PTA) catheters ... Balloon Material on a 4 french system. It is available in 4 - 7mm diameters and 1.5 - 4cm lengths ...

The FDA determined this week that Cordis’ recent recall of several versions of its Super Torque angiographic catheters meet the criteria of a Class I recall, a label reserved for those the ...

Separately, Cordis said it was recalling its line of LuSee TLC Steerable Guidewires, single-use disposable devices that assist in the precise positioning of angioplasty catheters within coronary ...

SAN FRANCISCO--(BUSINESS WIRE)--Cordis Corporation today announced EMPIRA™ and EMPIRA™ NC RX PTCA Dilatation Catheters have received 510(k) regulatory clearance for the treatment of coronary ...

FREMONT, Calif.--(BUSINESS WIRE)-- Cordis Corporation today announced it has received clearance from the Food and Drug Administration of its latest innovation in guiding catheters: the ADROIT TM 6F ...

Cordis’ addition of the Chocolate ® PTA Balloon Catheter complements and expands ... in Western Europe and North America have PAD. 2-4 About Cordis Corporation ...

BRIDGEWATER, N.J.--(BUSINESS WIRE)-- Cordis Corporation is pleased to announce the launch of SLEEK® OTW Catheter, a new .014” Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter ...

Cordis Corp., Johnson & Johnson's stenting arm, notched another 510(k) clearance for its Adroit 6F Guiding Catheter, which the company says can handle more sophisticated lesions. Cordis Corp., the ...

In a sense, the workers are helping to save lives. The Cordis de Mexico plant makes catheters and stents used to treat various circulatory system problems for Cordis Corp., a Miami Lakes, Fla.-based ...

The Arklow-based manufacturer of cardiac intervention devices has agreed to supply its latest balloon catheter to the US group's Cordis subsidiary ... it raised a further €4.4 million in a ...