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Terumo Accuforce PTCA Dilatation Catheter (BD 2.50)

Terumo Accuforce PTCA Dilatation Catheter (BD 2.50)

Product Details:

  • Storage Instructions Store in Cool, Dry Place
  • Measurement Range Balloon Diameter: 2.50 mm
  • Accuracy High Precision Balloon
  • Instruments Type Cardiovascular Catheter
  • Features High Pushability and Trackability
  • Shelf Life 5 Years
  • Usage Type Single Use
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Terumo Accuforce PTCA Dilatation Catheter (BD 2.50) Price And Quantity

Terumo Accuforce PTCA Dilatation Catheter (BD 2.50) Product Specifications

  • No
  • Balloon Diameter: 2.50 mm
  • High Pushability and Trackability
  • Store in Cool, Dry Place
  • Balloon Angioplasty
  • High Precision Balloon
  • Medical Grade Polymer
  • Standard Length: 140 cm
  • Yes
  • Coronary Angioplasty
  • New
  • Single Use
  • Manual
  • 5 Years
  • Cardiovascular Catheter
  • Transparent/Clear
  • Lightweight
  • Silent
  • Yes
  • PTCA Dilatation Catheter
  • Dilatation of Coronary Arteries

Product Description

Brand Terumo
Ballon Diameter (mm) 2.50
Ballon Length (mm) 8, 12, 15, 20 & 25
CAT No. DC-RM2508HSW, DC-RM2512HHW, DC-RM2515HHW, DC-RM2520HHW & DC-RM2525HHW
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.



Superior Precision Balloon Technology

The Terumo Accuforce PTCA Dilatation Catheter uses a semi-compliant balloon technology, crafted for accurate and effective coronary artery dilatation. The high precision balloon with a 2.50 mm diameter offers optimal expansion, ensuring minimized vessel trauma and maximizing procedural success, even in complex lesions.


Safety and Ease of Use

Engineered with a tapered, atraumatic tip and manufactured from medical grade polymer, the Accuforce BD 2.50 traverses even intricate coronary anatomies with remarkable pushability and trackability. Ethylene oxide sterilization and individual sterile packaging further guarantee patient safety and infection control, adhering to global medical standards.


Adaptable and Reliable Performance

With compatibility for 0.014-inch guidewires and a rated burst pressure up to 20 atm, this PTCA catheter supports a broad range of clinical requirements. Its lightweight nature, standard 140 cm length, and absence of accessories make it both portable and simple to integrate into angioplasty procedures.

FAQs of Terumo Accuforce PTCA Dilatation Catheter (BD 2.50):


Q: How is the Terumo Accuforce PTCA Dilatation Catheter (BD 2.50) used during coronary angioplasty?

A: The catheter is introduced into the coronary artery over a 0.014-inch guidewire. The balloon is positioned precisely at the site of the arterial narrowing and inflated to the required pressure, dilating the blockage and restoring blood flow.

Q: What benefits does the semi-compliant balloon material provide?

A: The semi-compliant balloon adapts gently to vessel contours, allowing controlled, targeted dilatation with reduced risk of vessel injury. It ensures precision in expansion, particularly crucial in delicate or calcified lesions.

Q: When should I choose the BD 2.50 model for my procedure?

A: You should select the BD 2.50 model when a 2.50 mm balloon diameter is required to match the target coronary artery size during PTCA. Its standard lengths and compliant design provide versatility for a range of clinical scenarios.

Q: Where should the catheter be stored before use?

A: Store the catheter in a cool, dry place in its original sterile packaging to maintain sterility and integrity. Avoid exposure to direct sunlight or moisture, as this may compromise packaging and product quality.

Q: What is the sterility method for the Accuforce BD 2.50 catheter?

A: The Accuforce BD 2.50 catheter is sterilized using ethylene oxide, a method that ensures thorough sterilization while maintaining product material integrity and patient safety.

Q: How does the catheters tapered, atraumatic tip improve the procedure?

A: The tapered, atraumatic tip enhances navigation through complex vasculature, minimizing vessel trauma. This design reduces the risk of arterial dissection and facilitates precise balloon placement in the target lesion.

Q: What makes this catheter suitable for single-use cardiovascular interventions?

A: Its single-use design, CE Marking, and individually packed sterile pouch ensure each unit is uncontaminated and compliant with international safety standards, supporting optimal patient outcomes in coronary angioplasty.

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