Please provide your email address to receive an email when new articles are posted on . The FDA has designated a recall of a peripheral catheter system as class I, the most serious kind. Teleflex and ...

Current recommendations that a central catheter is required for continuous intravenous infusion of 3 percent sodium chloride solution should be re-evaluated, according to a study in the American ...

CAESAREA, Israel & TAMPA, Fla.--(BUSINESS WIRE)--Upstream Peripheral Technologies announced today that its CTO-busting GoBack® Catheter for crossing and reentry was proven very effective for patients ...

To report the experience of peripheral insertion of double-lumen central catheters (PIDLCC) in preterm and term newborn infants and to analyze the technical characteristics of the procedure and any ...

WAYNE, Pa.--(BUSINESS WIRE)--Teleflex Incorporated (NYSE:TFX), a global provider of medical devices for critical care and surgery, announced today that its ARROW Endurance™ Extended Dwell Peripheral ...

The case report by Vasquez et al. 1 describing the treatment of peripheral artery catheter-induced ischemic injury with topical nitroglycerin ointment in a newborn infant was interesting. Although the ...

ARTHESYS has announced the renewal of the CE mark of its LYNX RX PTA peripheral balloon catheter. The LYNX catheter comes in various options: either as plain dilation catheter, as stent delivery ...

The FDA cleared Medtronic’s angled support catheter for use in the treatment of peripheral artery disease, the company announced Wednesday. Support catheters are used in endovascular procedures to ...

MINNEAPOLIS, Minnesota -- Vascular Solutions, Inc. announces the immediate availability of the SuperCross™ microcatheter. The SuperCross offers superior crossability, flexibility, and exceptional ...

Covidien's Fortrex percutaneous transluminal angioplasty balloon catheter--Courtesy of Covidien Covidien ($COV) today announced FDA 510(k) clearance for its Fortrex ...