The Magellan™ 10Fr Robotic Catheter has received CE Marking for use in peripheral vascular procedures. The 10Fr catheter has the largest inner lumen (7Fr) in the Magellan catheter family, and enables precise delivery of therapeutic devices through a stable, robotic catheter platform in a broader range of Vascular procedures. View the official press release for more info.
Hansen Medical will be in booth # 221 at CX2015 in London, April 28 - May 1. Click to schedule a test drive with the 6Fr, 9Fr, or the new 10Fr Magellan Robotic Catheters. Thirteen different presentations will discuss Intravascular Robotics, including featured talks in the Main Programme, CX Imaging Day Parallel Session, and an educational speaker series in the Hansen booth. The full schedule of robotic talks can be found here.
Sandeep Rao, MD, Interventional Radiologist at Sierra Providence Health Network in El Paso, Texas presented data at the 2015 Society of Interventional Radiology (SIR) meeting showing 95% reduction to the operator in radiation during robot-assisted Transarterial Chemoembolization (TACE) procedures. with the Magellan™ Robotic System. Read more on the Hansen blog.
"Hansen Medical," "Hansen Medical (with Heart Design)," and "Heart Design (Logo)" are registered trademarks, and "Magellan" is a trademark of Hansen Medical, Inc. in the US and other countries. All other trademarks are the property of their respective owners.
Indications for Use
The Magellan™ Robotic System, Magellan Robotic Catheter and accessory components are intended to be used to facilitate navigation to anatomical targets in the peripheral vasculature and subsequently provide a conduit for manual placement of therapeutic devices.
Important Safety Information
As with most invasive procedures, use of the Magellan Robotic System is not without risk. Serious adverse events, some of which can be fatal, may occur, including vascular damage, embolization and stroke. Other potential risks inherent to procedures such as this include loss of limb, catheter entrapment, infection and access site complications (e.g. hematoma) which may require additional surgery.
Do not use the system without understanding the instructions for use. For information regarding, contraindications, warnings, precautions, adverse events, and methods of use, please see package inserts included with the product.