
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 EUP22510X) is a 2.25 mm x 10 mm coronary balloon catheter engineered to support percutaneous coronary intervention (PCI) workflows. Designed for rapid exchange delivery, the Euphora platform combines a low-profile tip with a semicompliant balloon intended to facilitate lesion crossing and controlled dilatation.
Key Features
- Semicompliant balloon material for predictable growth characteristics
- Balloon diameter 2.25 mm, balloon length 10 mm
- Rapid exchange (monorail) catheter design
- Low crossing profile tip to aid navigation through tight or tortuous anatomy
- Hydrophilic coating on distal shaft to support deliverability
- Dual radiopaque markers for fluoroscopic balloon positioning
- Nominal and rated burst pressure values: Not specified in the located sources
Clinical Applications
- Balloon dilatation of stenotic coronary lesions during PCI
- Pre-dilatation prior to stent deployment
- Post-dilatation and stent optimization
- Treatment of small-vessel coronary disease where a 2.25 mm working diameter is appropriate
- Use within native coronary arteries and coronary bypass grafts where clinically indicated by the treating physician
Product Information
- Brand: Medtronic
- Product Line: Euphora Rapid Exchange Semicompliant Balloon Dilatation Catheter
- REF / UPN: EUP22510X
- Balloon Diameter: 2.25 mm
- Balloon Length: 10 mm
- Delivery System: Rapid exchange (monorail)
- Balloon Compliance: Semicompliant
- Guidewire Compatibility: 0.014 in guidewire (standard for platform); confirm with current IFU
- Guide Catheter Compatibility: Not specified in the located sources
- Usable Catheter Length: Not specified in the located sources
- Sterility: Supplied sterile, single use
- Category: Coronary Balloon Catheters
- Regulatory status, clinical indications, and pressure ratings should be verified against the current manufacturer IFU for the buyer's region.
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