The Boston Scientific Sterling Balloon Catheter (REF H74939031603010) is a percutaneous transluminal angioplasty (PTA) balloon dilatation catheter featuring a 6 mm nominal balloon diameter and 30 mm balloon length. The Sterling platform is engineered to deliver a balance of pushability, trackability, and crossability for peripheral vascular interventions, with a low-profile balloon designed to navigate tortuous anatomy and tight lesions.
Key Features
- Nominal balloon diameter: 6 mm
- Balloon working length: 30 mm
- Semi-compliant balloon material engineered for predictable inflation
- Low crossing profile to facilitate lesion access
- Hydrophilic coating on the distal shaft to support trackability
- Two radiopaque marker bands for fluoroscopic balloon positioning
- Over-the-wire (OTW) design for guidewire support during exchanges
- Guidewire compatibility: Not specified in the located sources
- Recommended sheath/introducer size: Not specified in the located sources
- Rated burst pressure (RBP): Not specified in the located sources
Clinical Applications
- Percutaneous transluminal angioplasty of peripheral arteries
- Dilatation of stenoses in iliac, femoral, popliteal, infra-popliteal, and renal vasculature, where indicated by the operator
- Post-dilatation of balloon-expandable and self-expanding stents, where indicated
- Treatment of obstructive lesions in native or synthetic arteriovenous dialysis fistulae, where indicated
Specific indications, contraindications, warnings, and precautions are defined in the manufacturer Instructions for Use (IFU).
Product Information
- Brand: Boston Scientific
- Product line: Sterling Balloon Dilatation Catheter
- Category: Peripheral Balloon Catheters
- REF / UPN: H74939031603010
- Balloon size: 6 mm x 30 mm
- Catheter working length: Not specified in the located sources
- Sterility: Supplied sterile, single-use device
- Storage: Store as directed in the manufacturer IFU
- Packaging quantity: Refer to manufacturer packaging
Product specifications, availability, and regulatory status may vary by region; verify configuration and approved indications with the manufacturer prior to procurement.