Members only
Only the abluminal surface of the stent receives SMS treatment, allowing BA9™ to be contained within the micro-structured surface
and delivered with high specificity to the vessel wall of the coronary lesions.
 
The SMS process allows for an increased surface area for a uniform dose of BA9™ to be delivered to the target lesion.
 
With no need for polymer or carrier, BA9™ and SMS make BioFreedom™ a true Drug-Coated Stent (DCS).
 

Drug-Coated Stent

11522-000-EN - Rev.01 + 11881-000-EN - Rev.04
BioFreedom™
Movie - How does it work?
Watch the working principle of BioFreedom™
BioFreedom™
SMS brochure

BIOFREEDOM™ FAMILY CLINICAL PROGRAM

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The law restricts these devices to sale by or on the order of a physician. Prior to use, it is important to read the "Instructions for Use" supplied with these devices for indications, contraindications, suggested procedures, warnings, and precautions.

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.