
Boston Scientific Express Vascular LD Stent 6 x 17 mm | REF H74938162620750
Boston Scientific Express Vascular LD balloon-expandable peripheral stent, 6 mm diameter x 17 mm length, premounted on a delivery system (REF H74938162620750).

The Boston Scientific Epic Nitinol Vascular Stent (8 x 60 mm, REF H74939054086070) is a self-expanding peripheral stent constructed from nitinol and pre-mounted on a dedicated over-the-wire delivery catheter. The Epic platform is engineered to combine flexibility, conformability and sustained radial force for use in tortuous peripheral vasculature.
Key Features
Self-expanding nitinol architecture for thermal shape recovery and consistent radial force.
Tantalum radiopaque markers at stent ends for fluoroscopic visualization.
Closed-cell-influenced design intended to support vessel scaffolding while preserving flexibility.
Pre-loaded on an over-the-wire delivery system compatible with 0.035 in guidewires.
Triaxial delivery system designed for controlled, accurate deployment.
Single-use, sterile (ethylene oxide) packaging.
Clinical Applications
Indicated uses, vessel selection and patient suitability must be confirmed against the current manufacturer Instructions for Use (IFU) and applicable local regulatory clearances. The Epic stent family is generally positioned by the manufacturer for peripheral vascular applications including iliac arterial and venous segments. Final clinical decision making remains with the treating physician.
Product Information
Brand: Boston Scientific
Product Line: Epic Vascular Self-Expanding Stent System
REF / UPN: H74939054086070
Stent Diameter: 8 mm
Stent Length: 60 mm
Stent Material: Nitinol with tantalum markers
Delivery System: Over-the-wire, 0.035 in guidewire compatible
Usable Catheter Length: Not specified in the located sources
Introducer Sheath Compatibility: Not specified in the located sources
Sterilization: Ethylene oxide
Use: Single use, do not resterilize
Category: Peripheral Stents
Regulatory status, indications and contraindications: Refer to current manufacturer IFU and local regulatory documentation.
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