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Philips Vesper Medical
5905 Nathan Ln N
Plymouth, MN 55442

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CAUTION: Investigational Device. Limited by Federal (United States) law to investigational use.

Vesper DUO Venous System (DUO-HYBRID Stent) is CE Mark authorized under EC Directive 93/42/EEC for treating symptomatic obstructions of the iliac vein near the bifurcation of the inferior vena cava. Vesper DUO Venous Stent System (DUO-EXTEND Stent) is exclusively for clinical investigations.

Vesper DUO Venous Stent System^®, Vesper DUO EXTEND Venous Stent System^®, DUO-HYBRID™ and DUO-EXTEND™ are trademarks of Vesper Medical, Inc.

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