OTW Balloon Boston

OTW Balloon Boston 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 OTW Balloon Boston

The Mustang„ Over-The-Wire (OTW) Balloon Dilatation Catheter by Boston Scientific is engineered for percutaneous transluminal angioplasty (PTA) procedures, offering a combination of performance and versatility.

Key Features:

Powerful Dilatation: Designed to withstand up to 24 atmospheres of rated burst pressure, ensuring effective vessel expansion.

Low Profile: Features a low entry profile, with the tip only 15% larger than a 0.035-inch wire, facilitating easier navigation through vascular structures.
Broad Size Matrix: Offers a comprehensive range of sizes, with 203 code options, to accommodate various clinical requirements.
Enhanced Deliverability: The catheter's design ensures superior crossability and trackability, allowing for efficient navigation through complex anatomies.
Product Specifications:

Sizes: Available in diameters ranging from 2.0 mm to 12.0 mm and lengths from 20 mm to 200 mm.
Sheath Compatibility: Designed to be compatible with 5F to 7F sheaths, depending on the balloon size.

Indications for Use:

The Mustang„ OTW Balloon Dilatation Catheter is intended for:

Balloon dilation of the stenotic portion of a coronary artery or bypass graft stenosis to improve myocardial perfusion.
Balloon dilation of a coronary artery occlusion to restore coronary flow in patients with ST-segment elevation myocardial infarction.
Balloon dilation 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.