
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 Firefighter NC PTCA Balloon Catheter (REF FNC2520) is a rapid-exchange, non-compliant coronary balloon catheter with a nominal balloon diameter of 2.5 mm and a working length of 20 mm. It is engineered for predictable high-pressure inflation, supporting post-dilatation of deployed coronary stents and the treatment of resistant or calcified lesions during percutaneous coronary intervention (PCI).
Key Features
- Non-compliant balloon material for minimal diameter growth at elevated pressures
- Balloon size: 2.5 mm diameter x 20 mm length
- Rapid-exchange (monorail) shaft design for single-operator handling
- Low-profile balloon intended to support crossing of tight or previously stented segments
- Hydrophilic distal shaft coating to assist trackability and deliverability
- Dual radiopaque markers to aid fluoroscopic positioning
- Guidewire compatibility: 0.014 in (0.36 mm)
- Guiding catheter compatibility: Not specified in the located sources
- Nominal and rated burst pressure: Not specified in the located sources
Clinical Applications
- Post-dilatation and optimization of deployed coronary stents
- High-pressure dilatation of resistant, fibrotic or calcified coronary lesions
- Adjunctive balloon dilatation during complex PCI procedures
- Use in native coronary arteries and saphenous vein bypass grafts where clinically indicated
Product Information
- Brand: MicroPort
- Product family: Firefighter NC
- Category: Coronary Balloon Catheters
- Device type: Non-compliant PTCA balloon catheter, rapid-exchange
- REF / UPN: FNC2520
- Balloon diameter: 2.5 mm
- Balloon length: 20 mm
- Usable catheter length: Not specified in the located sources
- Sterilization: Supplied sterile, single-use (ethylene oxide per manufacturer labeling)
- Packaging: Individually packaged; refer to manufacturer IFU for unit quantity
- Regulatory status and approved indications: Refer to the manufacturer Instructions for Use and local regulatory labeling
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