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IDEV Technologies Announces First U.S. Procedure
with SUPERA VERITAS™ Transhepatic Biliary System
Commercial Launch of Stent Delivery System Planned for Early 2011
Webster, TX,
November 30, 2010 – IDEV Technologies, Incorporated (IDEV), an innovative leader in the
development and commercialization of minimally invasive medical technologies, today announced the first
procedure in the United States utilizing the SUPERA VERITAS™ Transhepatic Biliary System, which was
recently cleared to market by the U.S. Food and Drug Administration.
The SUPERA® wire interwoven nitinol stent is currently cleared in the U.S. for palliative treatment of biliary
strictures produced by malignant neoplasms. Biliary strictures involve a narrowing of the bile duct, the body's
transportation system for fluid that is an essential aid to the digestion of food. Stents are commonly used to
reopen the bile duct and restore the natural flow of fluids.
Mark Garcia, M.D., FSIR, is Chief of Interventional Radiology at Christiana Care Health System in Newark,
Delaware. He is the first physician in the U.S. to treat a patient's biliary stricture with the new SUPERA
VERITAS system. "The SUPERA's high radial strength is uniquely suited for treating biliary strictures. Because
of its characteristics, I've deployed a number of SUPERA stents over the past year. This new delivery system
worked flawlessly. The driving mechanism was smooth and very responsive. The post-procedure images
revealed optimal stent placement with excellent cholangiographic results and patency. I'm very pleased with
the result."
"We're thrilled to get positive feedback on the initial deployment of the SUPERA VERITAS system in the U.S.,"
commented Christopher M. Owens, President and CEO of IDEV. "Dr. Garcia's experience mirrors that of our
customers in Europe and Canada, where the SUPERA VERITAS system has been in use for the past year.
The stent's radial strength and flexibility combine to produce extremely high fracture resistance, and may
redefine how patients are treated."
Full commercial launch of the SUPERA VERITAS Transhepatic Biliary System is planned for the first quarter of
2011.
About IDEV Technologies, Incorporated
IDEV Technologies, Incorporated (IDEV) is an innovator and developer of next generation medical devices for
use in interventional radiology, vascular surgery and cardiology. IDEV's worldwide headquarters is located in
Webster, Texas and its European headquarters is located in Beuningen, The Netherlands. Please visit
www.idevmd.com.
The SUPERA stent is currently indicated in the U.S. for the palliative treatment of biliary strictures produced by
malignant neoplasms and in Europe for the treatment of biliary strictures produced by malignant neoplasms
and for peripheral vascular use following failed percutaneous transluminal angioplasty (PTA).
Contact: Donna Lucchesi
Vice President Global Marketing
IDEV Technologies, Incorporated
(281) 525-2000
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