
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 RX Semicompliant Balloon Dilatation Catheter (REF SPL32520X) is a rapid-exchange (RX) percutaneous transluminal coronary angioplasty (PTCA) catheter featuring a 3.25 mm nominal balloon diameter and 20 mm balloon working length. Engineered with a low-profile semicompliant balloon and a tapered tip, it is intended to support reliable crossability, trackability and predictable balloon growth during coronary interventions.
Key Features
- Semicompliant balloon material for predictable compliance behavior across the working pressure range
- Rapid-exchange (monorail) shaft design for single-operator handling
- Low entry profile and tapered distal tip to support lesion crossing
- Hydrophilic distal shaft coating to facilitate navigation through tortuous anatomy
- Two radiopaque marker bands for fluoroscopic visualization of balloon working length
- Balloon size: 3.25 mm x 20 mm
- Nominal and rated burst pressures: Not specified in the located sources
Clinical Applications
- Pre-dilatation of stenotic coronary lesions prior to stent deployment
- Post-dilatation and optimization of deployed coronary stents
- Balloon dilatation in native coronary arteries and bypass graft lesions
- Treatment of in-stent restenosis as part of a PCI strategy
- Adjunctive use during complex percutaneous coronary intervention procedures
Product Information
- Brand: Medtronic
- Product line: Sprinter Legend RX
- Category: Coronary Balloon Catheters
- REF / UPN: SPL32520X
- Balloon type: Semicompliant, rapid-exchange PTCA balloon
- Balloon diameter: 3.25 mm
- Balloon length: 20 mm
- Usable catheter length: Not specified in the located sources
- Guidewire compatibility: Not specified in the located sources
- Guide catheter compatibility: Not specified in the located sources
- Sterility: Supplied sterile, single-use device
- Regulatory status and clinical suitability: Refer to the manufacturer's Instructions for Use and local regulatory clearance in the destination market
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