Terumo Accuforce PTCA Dilatation Catheter (BD 3.25)

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Product Details:

Accuracy Precise Balloon Placement
Instruments Type Intravascular Catheter
Shelf Life Up to 2 Years (unopened)
Storage Instructions Store in a cool, dry place
Usage Type Single Use
Measurement Range Balloon diameter: 3.25 mm
Features Semi-compliant balloon, radiopaque markers, tapered distal tip
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Terumo Accuforce PTCA Dilatation Catheter (BD 3.25) Price And Quantity

Terumo Accuforce PTCA Dilatation Catheter (BD 3.25) Product Specifications

Equipment Type PTCA Dilatation Catheter
Shelf Life Up to 2 Years (unopened)
Operating Type Manual
Usage Type Single Use
Portable Yes
Storage Instructions Store in a cool, dry place
Condition Sterile, Disposable
Technology Balloon Angioplasty Technology
Material Medical Grade Polymer
Measurement Range Balloon diameter: 3.25 mm
Weight Lightweight
Function Dilatation of coronary arteries
Wall Mounted No
Real-Time Operation Yes
Accuracy Precise Balloon Placement
Instruments Type Intravascular Catheter
Dimension (L*W*H) Length: 140 cm (catheter)
Features Semi-compliant balloon, radiopaque markers, tapered distal tip
Use Coronary Artery Disease Treatment
Color Transparent/White (with colored markers)

Product Description

Brand	Terumo
Ballon Diameter (mm)	3.25
Ballon Length (mm)	12 & 20
CAT No.	DC-RM3212HHW & DC-RM3220HHW
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.

Advanced Balloon Angioplasty Technology

Leveraging medical-grade polymer and semi-compliant balloon technology, the Accuforce BD 3.25 delivers effective dilation of coronary arteries with reduced risk of vessel trauma. The balloon's compliance ensures controlled expansion, minimizing the potential for over-inflation and promoting safer outcomes for patients.

Designed for Precision and Safety

Featuring two radiopaque marker bands and a low-tip entry profile, this catheter allows for efficient and precise balloon placement. The flexible, kink-resistant shaft design improves maneuverability in challenging anatomies, further enhancing safety and procedural control during coronary interventions.

FAQ's of Terumo Accuforce PTCA Dilatation Catheter (BD 3.25):

Q: How is the Terumo Accuforce PTCA Dilatation Catheter used during a coronary angioplasty procedure?

A: The catheter is introduced into the coronary artery using a compatible 0.014" (0.36 mm) guidewire. It is advanced to the target site, where the semi-compliant balloon is inflated manually to dilate narrowed vessel segments, restoring blood flow as part of coronary artery disease treatment.

Q: What are the main benefits of using the Accuforce BD 3.25 compared to other catheters?

A: Its semi-compliant balloon provides controlled dilation, while radiopaque markers and a low-tip entry profile ensure accurate placement. The flexible, kink-resistant shaft enhances navigation, reducing procedure time and improving safety throughout angioplasty.

Q: When should this catheter be used and what conditions does it treat?

A: This device is indicated for use during percutaneous transluminal coronary angioplasty (PTCA) to dilate coronary arteries affected by atherosclerotic lesions, helping manage symptoms or complications of coronary artery disease.

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

A: To maintain sterility and shelf life, these catheters should be stored in a cool, dry place, in their individually packed sterile pouch, away from direct sunlight and moisture.

Q: What process ensures the sterility and safety of the Accuforce BD 3.25 Catheter?

A: Each catheter undergoes ethylene oxide sterilization and is packaged in a sealed, sterile pouch. The product is latex-free, minimizing the risk of allergies, and each unit's expiry date is clearly indicated on the packaging to ensure safe usage.

Q: Can the Accuforce BD 3.25 Catheter be reused for multiple procedures?

A: No, this catheter is designed strictly for single-use. After the procedure, it should be disposed of according to medical waste protocols to maintain patient safety and prevent cross-contamination.

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