
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 EUP2010X) is a 2.00 mm x 10 mm coronary balloon catheter designed for percutaneous transluminal coronary angioplasty (PTCA). It features a rapid exchange (monorail) shaft configuration intended to support efficient lesion access and balloon delivery during coronary interventions.
Key Features
Semicompliant balloon material intended to provide predictable inflation characteristics.
Rapid exchange (Rx) shaft platform for single-operator use.
Low-profile balloon design intended to support crossing of tight and tortuous lesions.
Balloon diameter: 2.00 mm; balloon length: 10 mm.
Tapered distal tip intended to support lesion access.
Hydrophilic coating on the distal shaft (as described by the manufacturer for the Euphora platform).
Radiopaque marker(s) to aid fluoroscopic positioning.
Rated burst pressure and nominal pressure: Not specified in the located sources.
Clinical Applications
Balloon dilatation of a stenotic portion of a coronary artery or bypass graft during PTCA procedures.
Predilatation prior to stent deployment in small-vessel coronary anatomy.
Postdilatation of deployed coronary stents where compatible.
Treatment of selected complex lesion morphologies, subject to operator assessment.
Product Information
Brand: Medtronic
Product Line: Euphora Semicompliant Balloon Dilatation Catheter
Catalog Reference (REF/UPN): EUP2010X
Category: Coronary Balloon Catheters
Shaft Configuration: Rapid Exchange (Rx / Monorail)
Balloon Type: Semicompliant
Balloon Diameter: 2.00 mm
Balloon Length: 10 mm
Usable Catheter Length: Not specified in the located sources
Guidewire Compatibility: Not specified in the located sources
Guide Catheter Compatibility: Not specified in the located sources
Sterility: Supplied sterile, single-use (as typical for the device category; confirm with current IFU)
Regulatory Status: Refer to current manufacturer labeling and regional regulatory documentation.
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