SELUTION SLR  Sirolimus Eluting PTCA Balloon Catheter   2.25 x 25 mm | REF SC14-225025

The Cordis SELUTION SLR Sirolimus Eluting PTCA Balloon Catheter (REF SC14-225025, 2.25 mm x 25 mm) is a rapid-exchange coronary drug-coated balloon engineered to deliver sirolimus to the vessel wall during percutaneous transluminal coronary angioplasty. The balloon surface is coated with MicroReservoirs comprising a biodegradable polymer intermixed with sirolimus, intended to provide a controlled and sustained release of the drug after a single inflation.

Key Features
- MicroReservoir technology with biodegradable polymer carrier for sustained sirolimus elution
- Sirolimus drug dose density: 1 microgram per square millimeter (per manufacturer literature)
- Rapid-exchange (monorail) catheter platform for 0.014 inch guidewires
- Semi-compliant balloon, 2.25 mm nominal diameter x 25 mm working length
- Hydrophilic coating on the distal shaft to support deliverability
- Radiopaque markers to aid fluoroscopic positioning of the working length

Clinical Applications
- Percutaneous coronary intervention in native coronary arteries
- Treatment scenarios where an operator selects a drug-coated balloon strategy, including small vessel disease and in-stent restenosis, in accordance with the approved Instructions for Use
- Use as part of a leave-nothing-behind interventional approach when clinically indicated by the treating physician

Product Information
Brand: Cordis
Product line: SELUTION SLR
Category: Coronary Balloon Catheters
REF / UPN: SC14-225025
Balloon diameter: 2.25 mm
Balloon length: 25 mm
Drug: Sirolimus
Drug dose density: 1 microgram per square millimeter
Catheter type: Rapid-exchange PTCA drug-coated balloon
Guidewire compatibility: 0.014 inch
Guide catheter compatibility: Not specified in the located sources
Usable catheter length: Not specified in the located sources
Nominal and rated burst pressures: Not specified in the located sources
Sterilization: Not specified in the located sources
Single use: Yes, single-patient use device per manufacturer labeling
Regulatory status and clinical indications: Refer to the current manufacturer Instructions for Use and local regulatory approvals in the destination market.

REF / UPNSC14-225025
Size2.25 x 25, 25 mm

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