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 ...
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 agency ...
DUBLIN, Ohio - Cordis, a Cardinal Health company, recently announced the full U.S. launch of its RADIAL 360 portfolio, offering a complete range of products to facilitate the transradial approach (TRA ...
Today at the 61st Annual Meeting of the Society for Vascular Surgery, Cordis Endovascular, division of Cordis Corporation, announced the worldwide launch of the Cordis AVIATOR(TM) Plus Balloon ...
Cordis, a unit of Johnson & Johnson, announced the launch of its SABER PTA Dilatation Catheter for the treatment of patients with Peripheral Arterial Disease. The SABER Catheter is cleared for use and ...
FREMONT, Calif.--(BUSINESS WIRE)-- Cordis Corporation announced the European CE marking and U.S. Food and Drug Administration (FDA) approval of additional sizes of its SLEEK® OTW platform, a 0.014 ...
FREMONT, Calif.--(BUSINESS WIRE)--Cordis Corporation announced today that it has entered into an agreement with TriReme Medical, Inc. that grants the company exclusive distribution rights for the ...
Please provide your email address to receive an email when new articles are posted on . Cordis Corporation has announced the clearance and launch of its Saber PTA dilatation catheter in the United ...
Medical devices group Clearstream Technologies has signed a landmark deal with US health care giant Johnson & Johnson. The Arklow-based manufacturer of cardiac intervention devices has agreed to ...
A view inside the Cordis Corporation plant in Miami Lakes. DANIEL BOCK FOR THE MIAMI HERALD With a key manufacturing plant in Miami Lakes, Cordis Corp. is one of the world’s leading designers and ...
January 25, 2008 (Miami Lakes, FL) - Cordis is recalling certain lots of its recently introduced Fire Star RX and Dura Star RX coronary balloon catheters because they pose a risk of "slow deflation or ...
Please provide your email address to receive an email when new articles are posted on . The FDA has identified Cordis’ recall of its angiographic catheter with radiopaque marker bands as Class I, the ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback