The packaging behind Medtronic’s EnVeoR Transcatheter Aortic Valve Implantation (TAVI) System offers an advancement from its predecessor, the CoreValve, according to a report by sister publication Packaging Digest, with the added functionality to the tray housing to the catheter within a sterile environment.
Surefire Medical, Inc. announced today that the company has received 510(k) FDA clearance to market its line of Surefire Angiographic Catheters. Surefire Medical will launch these products in the United States later this year.
The Arrow FlexTip Plus, the market-leading1 Open Tip, Single-Port epidural catheter, has been proven to significantly reduce complications commonly associated with epidural catheters, such as vein cannulations and paresthesia2-3. The Arrow FlexTip Plus Closed Tip, Multi-Port epidural catheter has been designed using the same proven technology of the Open Tip, Single-Port catheter, the only coil-reinforced catheter backed by more than a decade of clinical evidence.
TriReme Medical, Inc. (TMI) today announced approval by the U.S. Food and Drug Administration (FDA) of the Glider PTCA Catheter, indicated for treating the stenotic portion of coronary arteries or bypass grafts to improve myocardial perfusion.
Glider is the world's only torqueable PTCA balloon catheter. Combined with its state of the art tip technology, Glider is designed to perform, even in the most challenging conditions. It is also available in an ultra short balloon length of 4mm designed for focal lesions.