
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 MINI TREK II OTW Coronary Dilatation Catheter (REF 1012403-20A) is an over-the-wire percutaneous transluminal coronary angioplasty (PTCA) balloon catheter featuring a 2.0 mm diameter by 20 mm length semi-compliant balloon. Engineered for predilatation of stenotic coronary arteries, the MINI TREK II platform is built to deliver a low crossing profile and reliable pushability for accessing tight, calcified, or distal lesions during interventional cardiology procedures.
Key Features
- Balloon dimensions: 2.0 mm nominal diameter x 20 mm working length
- Catheter design: Over-the-wire (OTW) configuration supporting independent guidewire exchange and contrast/saline injection through the wire lumen
- Balloon material: Semi-compliant balloon designed for predictable inflation and lesion preparation
- Low entry and crossing profile intended to facilitate navigation through tight or tortuous coronary anatomy
- Hydrophilic coating on the distal shaft to support deliverability and lesion crossing
- Guidewire compatibility: 0.014 inch coronary guidewires
- Radiopaque markers for fluoroscopic balloon positioning
- Single-use, sterile (EO) packaged device
Clinical Applications
- Predilatation of stenotic lesions in native coronary arteries and bypass grafts
- Lesion preparation prior to stent deployment
- Use in cases where an OTW platform is preferred, such as distal wire support, wire exchange, or selective contrast injection distal to the lesion
- Postdilatation when an appropriately sized semi-compliant balloon is indicated
Product Information
- Brand: Abbott
- Product line: MINI TREK II OTW
- Category: Coronary Balloon Catheters / PTCA Dilatation Catheters
- REF / UPN: 1012403-20A
- Balloon size: 2.0 mm x 20 mm
- Platform: Over-the-Wire (OTW)
- Guidewire compatibility: 0.014 inch
- Nominal and rated burst pressures: Not specified in the located sources
- Usable catheter length: Not specified in the located sources
- Sterilization: Single-use, sterile
- Regulatory status and indications: Refer to the manufacturer Instructions for Use (IFU) and local regulatory labeling
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