CE mark approval for blueflow Venous Stent

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The blueflow Venous Stent (plus medica) received the CE mark in January 2018.

The news was announced via a company release in March.

The blueflow Venous Stent, developed and manufactured in Germany is a two nitinol wire braided stent used to treat venous outflow obstructions of the lower extremities.

“Its high flexibility gives the physician more treatment options below the inguinal ligament,” explains Georg Landsberg, founder and CEO plus medica.

Further, the release reports that the first cases are already scheduled at a dedicated venous centre.

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