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Xlumena Receives CE Mark for NAVIX™, Second Product to Enter European Market
Date:6/30/2011

tments of diseases that have been treated surgically in the past.  Xlumena is meeting this need with efficient, reliable solutions.  The NAVIX Access Device and the AXIOS Stent are examples of the type of tools that will fundamentally change the way therapy is delivered and improve patient care."

About the NAVIX Access Device

The NAVIX includes an endoscopic trocar that creates an initial incision into the pseudocyst, an anchor balloon that secures access within the pseudocyst, and a dilation balloon that expands the access tract to 10mm in diameter.  The NAVIX also enables placement of up to two guidewires into the pseudocyst, which can be used to deploy one or more drainage stents (guidewires and stents not included).  The NAVIX handle is ergonomically designed and allows the interventional endoscopist to deploy the device using a single hand. The NAVIX may also be used to create an access tract for placement of Xlumena's AXIOS Stent, which is the only drainage stent on the market in Europe specifically indicated for transmural pancreatic pseudocyst drainage. To view an animation of the NAVIX, visit http://www.vimeo.com/xlumena/navix.

About Xlumena

Xlumena is the leader in the development of image-guided therapeutic endoscopy products, specializing in advanced implants and devices for a new, rapidly growing field of medicine. Collaborating with top physicians in the field, Xlumena focuses on technologies that advance therapy to the next level. These innovations may enable numerous translumenal therapeutic procedures, helping transform complex surgeries into outpatient events.

To view an animation of Xlumena's first product available in Europe, the AXIOS Stent and Delivery System (CE Mark approved), visit http://www.vimeo.com/xlumena/axios.


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SOURCE Xlumena, Inc.
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