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Designed for in-stent restenosis:

The use of the BioStream™ PTCA catheter is indicated for patients with discrete lesions of the coronary arteries with a reference vessel diameter of 1.50 to 4.00 mm for the purpose of improving the coronary lumen diameter.
The BioStream™ PTCA catheter is indicated for the dilatation of the affected segments of a coronary artery or a coronary bypass in order to enhance myocardial perfusion. The BioStream paclitaxel eluting coronary balloon catheter is especially indicated for the treatment of coronary in-stent restenosis.

11239-000-EN – Rev.01 + 11881-000-EN - Rev.04
BioStream™
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BioStream™
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Biosensors’ interventional cardiology products, including BioMatrix NeoFlex™, BioMatrix™ Alpha, BioFreedom™, BioFreedom™ Ultra, Chroma™, BioStream™, BMX-J®, BioPath™, Powerline™, RISE™ NC, are not available for sale in the United States and certain other countries. ALLEGRA™ is a product of NVT AG. Blue Sail Medical Co., Ltd is the parent company of NVT AG and Biosensors International Group, Ltd. and its affliates are collaborating for the commercialization of the ALLEGRA™ device.

BioMatrix NeoFlex, BioMatrix Alpha, BioFreedom, BioFreedom Ultra, Chroma, BioStream, BMX-J, BioPath, Juno, S-Stent, Powerline, Rise NC and Quadrature Link are trademarks or registered trademarks of Biosensors International Group, Ltd. ALLEGRA is a trademark or registered trademark of NVT AG. ALLEGRA™ is CE Mark approved (CE 0124). All other cited trademarks are the property of their respective owners.