Balloon Dilatation Catheters: Powerline™

Take the Fast Track to Superior Patient Outcomes

The advanced catheter technology of Powerline™ is designed to offer the right balance of PUSH, TRACK and CROSS to ensure optimal balloon placement and expansion:


The PTFE-coated hypotube in combination with the power stylet transition in the middle shaft provides the right balance between pushability and trackability offering a smoother force transmission from the proximal to distal portion of the catheter shaft.


The combination of the Slip-X™ hydrophilic coating and the flexible distal shaft ensure excellent trackability and crossability for complex lesions or tortuous anatomy.


The flexible low profile tip section with smooth transition and short bonding offers a gradual increase towards the balloon to facilitate lesion entry. The advanced MultiPleat™ folding technology of Powerline™ is designed to offer exceptional lesion crossability and uniform balloon expansion as well as excellent balloon re-wrap and re-cross properties for treating challenging lesions.


MultiPleat™ Folding Technology

The MultiPleat™ folding technology is designed to facilitate the treatment of multiple lesions as the machine folding provides a more consistent rewrap of the balloon.

This fully automated mechanism offers exceptional lesion crossability and uniform balloon expansion, as well as improved re-cross properties that may facilitate complex procedures and reduce procedural time.

10408-000-EN - Rev.05 + 11881-000-EN – Rev.04
Main brochure

Ordering information

CAUTION: Please note that the following pages are exclusively reserved for Health Care Professionals in countries with applicable health authority product registrations. To the extent this site contains information intended for use by licensed medical professionals, such materials are not intended to offer professional medical advice. Prior to use, please consult device labeling for prescriptive information and operating instructions. Please contact your Biosensors International representative for availability or the products and registration status.

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.