
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 Medtronic Sprinter Legend OTW Semicompliant Balloon Dilatation Catheter (REF SPL12515WL) is an over-the-wire (OTW) percutaneous transluminal coronary angioplasty (PTCA) balloon catheter with a 1.25 mm balloon diameter and 15 mm balloon length. Engineered with a semicompliant balloon material, it is intended to support controlled, predictable inflation during coronary lesion preparation and dilatation procedures.
Key Features
Semicompliant balloon designed for predictable growth across the working pressure range.
Over-the-wire (OTW) catheter configuration supporting full-length guidewire control and exchanges.
Low-profile balloon tip engineered to facilitate crossing of tight or distal lesions.
Tapered tip geometry intended to support smooth lesion entry.
Radiopaque marker(s) to aid fluoroscopic balloon positioning.
Hydrophilic or low-friction shaft coating as specified by the manufacturer (refer to current IFU).
Compatible with standard 0.014 in coronary guidewires per the manufacturer's IFU.
Clinical Applications
Balloon dilatation of stenotic coronary lesions in native coronary arteries and bypass grafts.
Pre-dilatation of lesions prior to coronary stent deployment.
Post-dilatation and optimization of deployed coronary stents within labeled balloon pressure limits.
Treatment of small-vessel and tight, difficult-to-cross lesions where a 1.25 mm low-profile balloon is appropriate.
Use in standard and complex PCI workflows where OTW guidewire support or exchange capability is preferred.
Product Information
Brand: Medtronic
Product: Sprinter Legend OTW Semicompliant Balloon Dilatation Catheter
Category: Coronary Balloon Catheters
REF / UPN: SPL12515WL
Balloon Diameter: 1.25 mm
Balloon Length: 15 mm
Catheter Platform: Over-the-Wire (OTW)
Balloon Compliance: Semicompliant
Guidewire Compatibility: 0.014 in coronary guidewire (refer to IFU)
Nominal and Rated Burst Pressure: Not specified in the located sources; refer to the current Medtronic IFU and product label.
Usable Catheter Length: Not specified in the located sources; refer to the current Medtronic IFU.
Sterility: Supplied sterile, single-use device (refer to packaging and IFU).
Indication / Regulatory Status: Refer to the current Medtronic Instructions for Use and local regulatory clearance for approved indications in your region.
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