
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 SPL32515X) is a rapid exchange (RX) coronary balloon catheter featuring a 3.25 mm nominal balloon diameter and 15 mm working length. Engineered for predictable performance in percutaneous coronary intervention (PCI), it combines a low-profile balloon with a flexible shaft to support efficient lesion access and dilatation.
Key Features
- Semicompliant balloon material for controlled, predictable inflation characteristics
- Rapid exchange (monorail) design compatible with 0.014" guidewires
- Low crossing profile to facilitate navigation through tight or tortuous anatomy
- Tapered, flexible distal tip to support lesion entry
- Hydrophilic coating on the distal shaft to reduce friction (per manufacturer literature)
- Two radiopaque markers delineating the balloon working length under fluoroscopy
- Nominal diameter 3.25 mm; working length 15 mm
- Guide catheter compatibility: Not specified in the located sources
- Rated burst pressure and nominal pressure: 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 of de novo and restenotic lesions in native coronary arteries and bypass grafts as indicated by the operator
- Use in standard PCI workflows where a semicompliant balloon is preferred over a non-compliant device
Product Information
- Brand: Medtronic
- Product: Sprinter Legend RX Semicompliant Balloon Dilatation Catheter
- REF / UPN: SPL32515X
- Balloon Diameter: 3.25 mm
- Balloon Length: 15 mm
- Delivery System: Rapid Exchange (RX)
- Guidewire Compatibility: 0.014" coronary guidewires
- Category: Coronary Balloon Catheters
- Sterility / Single Use: Supplied sterile, single-use device (refer to manufacturer IFU)
- Regulatory status, indications, contraindications and full technical specifications: Refer to the official Medtronic Instructions for Use (IFU) and product labeling for the destination market.
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