The Boston Scientific Sterling Balloon Catheter (REF H74939147351590) is a low-profile, over-the-wire percutaneous transluminal angioplasty (PTA) balloon dilatation catheter designed for use in the peripheral vasculature. This configuration features a 3.5 mm nominal balloon diameter and a 150 mm balloon working length, intended to support controlled dilatation of stenotic lesions in small to medium peripheral vessels.
Key Features
Low-profile balloon design intended to facilitate crossing of tight lesions.
Nominal balloon diameter of 3.5 mm with a 150 mm working length for long-segment treatment.
Over-the-wire platform compatible with standard guidewires (refer to IFU for compatible guidewire diameter).
Balloon material engineered for predictable inflation and deflation characteristics.
Radiopaque markers to assist with fluoroscopic balloon positioning.
Hydrophilic coating segment to support trackability and lesion crossing (refer to IFU).
Clinical Applications
Indicated for percutaneous transluminal angioplasty procedures in the peripheral vasculature as described in the manufacturer's instructions for use.
Dilatation of stenotic lesions in small to medium peripheral arteries.
Post-dilatation in selected peripheral interventional workflows where supported by the IFU.
Refer to the official Boston Scientific Sterling IFU for the complete list of indications, contraindications, warnings, and precautions.
Product Information
Brand: Boston Scientific
Product Family: Sterling Balloon Dilatation Catheter
Category: Peripheral Balloon Catheters
Balloon Diameter: 3.5 mm (nominal)
Balloon Length: 150 mm
Catheter Platform: Over-the-wire PTA balloon catheter
Usable Catheter Length: Not specified in the located sources
Guidewire Compatibility: Not specified in the located sources
Minimum Introducer Sheath: Not specified in the located sources
Rated Burst Pressure: Not specified in the located sources
Nominal Pressure: Not specified in the located sources
Sterility: Supplied sterile for single use; do not resterilize
REF / UPN: H74939147351590
Regulatory Status: Refer to local regulatory labeling and the official manufacturer IFU prior to use.