
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 MicroPort Foxtrot NC PTCA Balloon Catheter (REF PH4008) is a non-compliant coronary dilatation catheter featuring a 4.0 mm nominal balloon diameter and 8 mm working length. Engineered for predictable, high-pressure inflation, the Foxtrot NC supports controlled lesion preparation and optimal stent expansion during percutaneous coronary intervention (PCI).
Key Features
- Non-compliant balloon material designed to maintain balloon geometry at high pressures.
- Nominal diameter: 4.0 mm.
- Balloon length: 8 mm for focal lesion treatment.
- Rapid exchange (monorail) shaft for single-operator handling over a 0.014" guidewire.
- Low crossing profile and tapered tip intended to facilitate crossing of tight or calcified lesions.
- Bi-directional hydrophilic-compatible shaft coating to support trackability and deliverability.
- Twin radiopaque markers indicating balloon working length under fluoroscopy.
- Rated Burst Pressure (RBP) and Nominal Pressure: Not specified in the located sources; refer to the manufacturer's Instructions for Use.
Clinical Applications
- Post-dilatation of deployed coronary stents to optimize apposition and expansion.
- Lesion preparation in resistant, fibrotic or calcified coronary stenoses.
- High-pressure dilatation of native coronary arteries and saphenous vein bypass grafts where clinically indicated.
- Treatment of in-stent restenosis as part of a broader interventional strategy.
Product Information
- Brand: MicroPort.
- Product line: Foxtrot NC PTCA Balloon Catheter.
- Reference / UPN: PH4008.
- Balloon size: 4.0 mm x 8 mm.
- Category: Coronary Balloon Catheters.
- Delivery system: Rapid exchange, 0.014" guidewire compatible.
- Guide catheter compatibility, shaft length, and sterilization method: Not specified in the located sources; confirm with the manufacturer's IFU and packaging.
- Single use, sterile device. Regulatory status and market availability vary by country; verify local approval prior to procurement.
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