Abbott Nc Trek Balloon

Abbott Nc Trek Balloon Trade Information

Minimum Order Quantity
100 Packs

FOB Port
AHMEDABAD

Payment Terms
Paypal, Cash Advance (CA), Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)

Delivery Time
3 Days

Sample Policy
Sample costs shipping and taxes has to be paid by the buyer

Packaging Details
Box

Main Export Market(s)
Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa

Main Domestic Market
All India

About Abbott Nc Trek Balloon

The Abbott NC TREK NEO„ Coronary Dilatation Catheter is a non-compliant balloon catheter designed for coronary artery procedures. It offers a broad size matrix, excellent pushability, and exceptional balloon performance, making it suitable for challenging anatomies.

Key Features:

Broad Size Matrix: Available in diameters ranging from 1.50 mm to 6.00 mm and lengths from 6 mm to 25 mm, accommodating various clinical needs.
Low Crossing Profile: The catheter's design ensures a lower crossing profile compared to previous models, facilitating easier navigation through coronary vessels.
Flat Compliance: The balloon maintains consistent expansion characteristics, providing uniform vessel wall apposition during inflation.
Fast Deflation Time: Quick deflation enhances procedural efficiency.

Indications for Use:

The NC TREK NEO„ Coronary Dilatation Catheter is indicated for:

Balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis to improve myocardial perfusion.
Balloon dilatation of a coronary artery occlusion to restore coronary flow in patients with ST-segment elevation myocardial infarction.
Balloon dilatation of a stent after implantation (for balloon models 2.00 mm “ 5.00 mm only).

Important Safety Information:

The device is intended for single use only. Do not re-sterilize or reuse, as this can compromise device performance and increase the risk of cross-contamination.
Percutaneous transluminal coronary angioplasty (PTCA) should only be performed at centers where emergency coronary artery bypass graft surgery is available.
Persons with known allergies to any components of this device may suffer an allergic reaction. A thorough history of allergies should be discussed prior to use.