
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 Abbott Sapphire II PRO Balloon Dilatation Catheter (REF 232-103-5UU) is a rapid-exchange semi-compliant PTCA balloon catheter with a nominal balloon diameter of 3.25 mm and a working length of 10 mm. Engineered for predictable lesion crossing and controlled dilatation, the Sapphire II PRO platform is designed to support a wide range of coronary interventions through a low-profile, trackable delivery system.
Key Features
- Semi-compliant balloon material with consistent inflation behavior across the working pressure range
- Low crossing profile engineered to facilitate access through tight or tortuous coronary anatomy
- Hydrophilic distal shaft coating intended to enhance lubricity and deliverability
- Rapid-exchange (monorail) design compatible with 0.014" guidewires
- Bi-directional radiopaque markers for fluoroscopic balloon positioning
- Tapered balloon shoulders intended to reduce edge dissection risk during dilatation
Clinical Applications
- Percutaneous transluminal coronary angioplasty (PTCA) of de novo or restenotic coronary lesions
- Pre-dilatation preparation of target lesions prior to stent deployment
- Post-dilatation optimization of deployed coronary stents
- Treatment of lesions in native coronary arteries and saphenous vein bypass grafts where balloon dilatation is indicated
Product Information
- Brand: Abbott
- Product Line: Sapphire II PRO
- Category: Coronary Balloon Catheters
- REF / UPN: 232-103-5UU
- Balloon Diameter: 3.25 mm
- Balloon Length: 10 mm
- Catheter Type: Semi-compliant PTCA balloon, rapid-exchange
- Guidewire Compatibility: 0.014"
- Nominal Pressure / Rated Burst Pressure: Not specified in the located sources
- Usable Catheter Length: Not specified in the located sources
- Sterility: Supplied sterile, single-use device
- Regulatory Status: Refer to the manufacturer's Instructions for Use (IFU) for indications, contraindications and approvals applicable to your region
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