
Synergy Shield Coronary Stent 2.50 X 8 | REF H7493966608250
Boston Scientific Synergy Shield Coronary Stent, 2.50 mm x 8 mm (REF H7493966608250) for B2B medical device procurement.

The Abbott Xience Xpedition Coronary Stent (REF 1070300-48) is a drug-eluting coronary stent system featuring a 3.00 mm × 48 mm everolimus-eluting stent premounted on a rapid-exchange delivery catheter. Engineered for deliverability in challenging coronary anatomy, the Xpedition platform is part of Abbott's established Xience family of everolimus-eluting stents used in percutaneous coronary intervention (PCI).
Key Features
- Stent diameter: 3.00 mm
- Stent length: 48 mm
- Drug coating: Everolimus eluted from a durable fluoropolymer-based coating
- Stent material: Cobalt chromium alloy (MULTI-LINK design)
- Delivery system: Rapid-exchange (Rx) balloon catheter
- Guidewire compatibility: 0.014 in (0.36 mm)
- Enhanced deliverability: Designed for improved pushability and trackability through tortuous vessels
- Single-use, sterile: Sterilized by ethylene oxide; do not resterilize
Clinical Applications
- Intended for use in percutaneous coronary intervention procedures
- Treatment of coronary artery lesions in vessels consistent with the 3.00 mm reference vessel diameter range
- Long-lesion coverage with a single 48 mm device to reduce the need for overlapping stents
- Suitable use, patient selection and indications must follow the current manufacturer Instructions for Use (IFU) and applicable local regulatory labeling
Product Information
- Brand: Abbott
- Product line: Xience Xpedition Everolimus Eluting Coronary Stent System
- Category: Coronary Stents / Drug-Eluting Stents (DES)
- REF / UPN: 1070300-48
- Configuration: 3.00 mm × 48 mm, premounted on Rx delivery catheter
- Packaging: Single sterile unit; refer to label for expiry and storage
- Storage: Store as indicated on packaging; keep dry and away from direct sunlight
- Regulatory status: Not specified in the located sources; buyers must verify regional approval and availability prior to procurement
- Prescription use: Restricted to qualified interventional cardiologists in accordance with local regulations and the manufacturer IFU
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