
AGENT Paclitaxel-Coated PTCA Balloon Catheter 2 X 12 | REF H74939222201210
Boston Scientific AGENT Paclitaxel-Coated PTCA Balloon Catheter, 2.0 mm x 12 mm (REF H74939222201210) — drug-coated balloon for coronary intervention.

The Cordis SELUTION SLR Sirolimus Eluting PTCA Balloon Catheter (REF SC14-375035, 3.75 mm x 35 mm) is a rapid-exchange coronary drug-coated balloon engineered for percutaneous transluminal coronary angioplasty (PTCA). It combines conventional balloon angioplasty with a sustained local release of sirolimus intended to limit neointimal proliferation, offering a leave-nothing-behind treatment option for selected coronary lesions.
Key Features
- Sirolimus-eluting PTCA balloon built on the SELUTION SLR MicroReservoir platform
- Biodegradable polymer MicroReservoirs designed for sustained, controlled sirolimus release to the vessel wall
- CAT (Cell Adherent Technology) intended to promote drug transfer and retention during inflation
- Rapid-exchange (monorail) catheter design for single-operator use
- Balloon size: 3.75 mm diameter x 35 mm length
- Low-profile balloon intended to support crossing and uniform drug delivery
- Radiopaque markers to aid fluoroscopic positioning
- Compatibility: Not specified in the located sources
Clinical Applications
- Percutaneous transluminal coronary angioplasty in native coronary arteries
- Local delivery of sirolimus during coronary balloon angioplasty procedures
- Use in interventional cardiology catheterization laboratories by trained operators following the manufacturer Instructions for Use
Product Information
- Brand: Cordis
- Product: SELUTION SLR Sirolimus Eluting PTCA Balloon Catheter
- REF / UPN: SC14-375035
- Balloon diameter: 3.75 mm
- Balloon length: 35 mm
- Drug: Sirolimus
- Delivery system: Rapid-exchange PTCA balloon catheter
- Category: Coronary Balloon Catheters
- Sterility, shelf life, nominal/rated burst pressures, guidewire and guide catheter compatibility: Not specified in the located sources
- Regulatory status: Availability and approved indications vary by country; refer to local regulatory labeling and the official Instructions for Use.
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