The Boston Scientific Sterling Balloon Catheter (REF H74939032602210) is a percutaneous transluminal angioplasty (PTA) balloon dilatation catheter featuring a 6 mm nominal balloon diameter and a 220 mm balloon working length. Engineered for peripheral vascular interventions, the Sterling platform is designed to deliver a balance of pushability, trackability, and crossing performance for the treatment of stenotic lesions in peripheral arteries.
Key Features
- Nominal balloon diameter: 6 mm
- Balloon length: 220 mm
- Semi-compliant balloon material engineered for predictable inflation characteristics
- Low-profile balloon designed to facilitate lesion crossing
- Hydrophilic coating on the distal shaft to support trackability (per manufacturer platform description)
- Radiopaque markers to aid fluoroscopic balloon positioning
- Monorail / rapid-exchange catheter configuration (per Sterling platform; confirm specific REF configuration with manufacturer)
- Guidewire compatibility: Not specified in the located sources for this specific REF; confirm with manufacturer IFU
- Working length: Not specified in the located sources for this specific REF
Clinical Applications
- Percutaneous transluminal angioplasty of stenotic lesions in the peripheral vasculature
- Dilatation of long-segment lesions where extended balloon length is indicated
- Post-dilatation following peripheral stent deployment, where clinically appropriate per operator judgment and the device IFU
- Refer to the official Instructions for Use for indications, contraindications, warnings, and precautions specific to this device.
Product Information
- Brand: Boston Scientific
- Product Family: Sterling Balloon Dilatation Catheter
- Category: Peripheral Balloon Catheters
- REF / UPN: H74939032602210
- Balloon Diameter: 6 mm
- Balloon Length: 220 mm
- Sterility: Supplied sterile for single use (confirm per IFU)
- Latex: Not specified in the located sources
- Rated Burst Pressure / Nominal Pressure: Not specified in the located sources for this specific REF; refer to the product compliance chart in the IFU