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Terumo Accuforce PTCA Dilatation Catheter (BD 3.50)

Terumo Accuforce PTCA Dilatation Catheter (BD 3.50)

Product Details:

  • Usage Type Single Use, Disposable
  • Shelf Life 3 years
  • Measurement Range Balloon diameter 3.50 mm
  • Function Dilation of narrowed coronary arteries
  • Instruments Type Interventional Cardiology Device
  • Features Radiopaque marker, flexible shaft, high-pressure capacity
  • Storage Instructions Store in a cool, dry place, away from direct sunlight
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Terumo Accuforce PTCA Dilatation Catheter (BD 3.50) Price And Quantity

Terumo Accuforce PTCA Dilatation Catheter (BD 3.50) Product Specifications

  • Medical Grade Polymer
  • Interventional Cardiology Device
  • Dilation of narrowed coronary arteries
  • Transparent with blue balloon
  • High precision for balloon inflation
  • No
  • Manual
  • Yes
  • Balloon diameter 3.50 mm
  • Yes
  • New
  • Semi-Compliant Balloon
  • 3 years
  • Coronary Angioplasty
  • PTCA Dilatation Catheter
  • Store in a cool, dry place, away from direct sunlight
  • Standard catheter length, varies by model (typically 140 cm)
  • Single Use, Disposable
  • Radiopaque marker, flexible shaft, high-pressure capacity
  • Lightweight, under 50 g
  • 3.50 mm
  • 15 mm (typical for BD 3.50, verify with product code)
  • Hydrophilic distal shaft coating
  • Semi-compliant polymer
  • Adult
  • Ethylene Oxide (EtO) sterilized
  • Sterile, single blister pack
  • 0.014 inch (0.36 mm)
  • 8-12 atm
  • Compatible with standard 6F or greater guiding catheters
  • Terumo Accuforce PTCA Dilatation Catheter BD 3.50
  • CE Marked, FDA cleared
  • 140 cm
  • 16 atm
  • 2 markers for precise placement
  • Stamped on packaging

Product Description

Brand Terumo
Ballon Diameter (mm) 3.50
Ballon Length (mm) 8, 12, 15 & 20
CAT No. DC-RM3508HSW, DC-RM3512HHW, DC-RM3515HHW & DC-RM3520HHW
Catheter Length (cm) 110

The great balance between high pressure and high resistance, accurate dilatation and advanced deliverability. Accuforce is the latest generation of non-compliant PTCA balloons.



Enhanced Precision in Angioplasty

The Terumo Accuforce PTCA Dilatation Catheter BD 3.50 integrates a semi-compliant balloon and radiopaque markers, offering high accuracy during inflation and placement. Its hydrophilic coating enhances maneuverability even in challenging anatomies, supporting interventional cardiologists with controlled balloon expansion and reliable vascular access.


Compatibility and User-Friendly Design

This catheter boasts compatibility with standard 6F or greater guiding catheters and 0.014-inch guidewires, streamlining its integration into established procedural workflows. Its lightweight, flexible shaft and transparent body with a blue balloon provide clear visual cues and ease of handling for efficient use during coronary interventions.

FAQ's of Terumo Accuforce PTCA Dilatation Catheter (BD 3.50):


Q: How is the Terumo Accuforce PTCA Dilatation Catheter BD 3.50 used during coronary angioplasty?

A: The catheter is inserted via a guiding catheter into the coronary artery. Its balloon is advanced to the site of narrowing, where it is inflated to stretch the vessel, allowing improved blood flow. Inflation is performed manually, guided by two radiopaque markers for precise positioning.

Q: What are the benefits of the hydrophilic distal shaft coating and dual radiopaque markers?

A: The hydrophilic coating reduces friction, making navigation through arteries smoother. The dual radiopaque markers provide enhanced visibility under fluoroscopy, ensuring accurate placement of the balloon during the procedure.

Q: When should the Terumo Accuforce PTCA Dilatation Catheter BD 3.50 be used, and who is the intended patient?

A: This catheter is designed for adult patients requiring dilation of coronary artery lesions during angioplasty. It is used when a physician determines balloon-based vessel expansion is needed to restore arterial blood flow.

Q: Where should the Terumo Accuforce PTCA Dilatation Catheter be stored before use?

A: Store this catheter in a cool, dry place, away from direct sunlight, to maintain sterility and product integrity until its expiry date, which is indicated on the packaging.

Q: What is the process for verifying compatibility with other instruments?

A: Ensure compatibility by using a 0.014-inch guidewire and a standard 6F or greater guiding catheter. The transparent body and semi-compliant balloon facilitate easy identification and setup during procedures.

Q: How does the semi-compliant balloon technology improve performance?

A: Semi-compliant balloon material allows controlled expansion at high pressures (up to 16 atm RBP). This helps achieve effective lesion dilation with minimized risk of vessel damage.

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