
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 Terumo Accuforce PTCA Dilatation Catheter (REF DC-RM3530HHW) is a rapid-exchange coronary balloon dilatation catheter featuring a 3.5 mm diameter by 30 mm length semi-compliant balloon. Engineered for controlled lesion dilatation during percutaneous transluminal coronary angioplasty (PTCA), the Accuforce platform is designed to combine pushability, trackability and refined crossing performance to support consistent device delivery through the coronary vasculature.
Key Features
- Semi-compliant balloon sized 3.5 mm x 30 mm for workhorse PTCA dilatation
- Rapid-exchange (monorail) shaft design for streamlined single-operator handling
- Low-profile balloon intended to assist crossing of tight or tortuous lesions
- Hydrophilic distal shaft coating to support smooth advancement and withdrawal
- Radiopaque markers to aid fluoroscopic positioning across the target segment
- Nominal and rated burst pressure values: 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 angioplasty in native coronary arteries and bypass grafts where clinically indicated
- Use by trained interventional cardiologists in catheterization laboratory settings
Product Information
- Brand: Terumo
- Product Line: Accuforce PTCA Dilatation Catheter
- REF / UPN: DC-RM3530HHW
- Balloon Diameter: 3.5 mm
- Balloon Length: 30 mm
- Category: Coronary Balloon Catheters
- Catheter Type: Semi-compliant PTCA dilatation balloon, rapid-exchange
- Guidewire Compatibility: 0.014 inch (typical for PTCA rapid-exchange systems; confirm with IFU)
- Guiding Catheter Compatibility: Not specified in the located sources
- Sterility: Supplied sterile, single use
- Packaging Quantity: Not specified in the located sources
Buyers should consult the official Terumo Instructions for Use and current regional regulatory documentation prior to procurement or clinical use.
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