
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 Euphora Rapid Exchange Semicompliant Balloon Dilatation Catheter (REF EUP37506X) is a coronary PTCA balloon catheter configured with a 3.75 mm nominal balloon diameter and a 6 mm balloon length. It is engineered for rapid exchange (monorail) delivery over a 0.014" guidewire and is intended to support predictable lesion preparation, balloon dilatation and stent post-dilatation during percutaneous coronary intervention (PCI) procedures.
Key Features
- Semicompliant balloon material formulated for a controlled compliance curve between nominal and rated burst pressure
- Rapid exchange (monorail) shaft design intended for single-operator workflow and quick balloon exchanges
- Low-profile balloon with tapered tip designed to support crossing of tight or calcified lesions
- Hydrophilic distal shaft coating intended to reduce friction during navigation through tortuous anatomy
- Two radiopaque markers under the balloon for fluoroscopic positioning at the target lesion
- 0.014" guidewire compatibility consistent with the Euphora platform
Clinical Applications
- Pre-dilatation of de novo stenotic coronary lesions prior to stent deployment
- Post-dilatation and optimization of deployed coronary stents
- Balloon dilatation in selected workhorse PCI cases requiring a short 6 mm balloon length
- Treatment planning where a 3.75 mm vessel diameter is targeted by the operator
Product Information
- Brand: Medtronic
- Product family: Euphora Semicompliant Rapid Exchange PTCA Balloon
- Category: Coronary Balloon Catheters
- REF / UPN: EUP37506X
- Balloon diameter: 3.75 mm (nominal)
- Balloon length: 6 mm
- Delivery system: Rapid exchange (monorail)
- Guidewire compatibility: 0.014"
- Balloon compliance: Semicompliant
- Usable catheter length: Not specified in the located sources
- Nominal and rated burst pressure: Not specified in the located sources
- Minimum guide catheter ID: Not specified in the located sources
- Sterility / single use: Supplied sterile, single use as indicated by the manufacturer's IFU
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