
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 1070300-12) is an everolimus-eluting coronary stent system pre-mounted on a rapid-exchange delivery catheter. This configuration provides a 3.00 mm expanded stent diameter and a 12 mm stent length, intended for percutaneous coronary intervention in adult patients. The device combines a cobalt chromium MULTI-LINK stent platform with a durable fluoropolymer-based coating that controls the release of everolimus.
Key Features
- Everolimus-eluting drug coating on a fluoropolymer carrier
- Cobalt chromium MULTI-LINK stent scaffold designed for low profile and conformability
- Pre-mounted on a rapid-exchange (Rx) delivery catheter for single-operator use
- Stent diameter 3.00 mm; stent length 12 mm
- Two radiopaque balloon markers to support fluoroscopic placement
- Supplied sterile for single use only
Clinical Applications
- Percutaneous coronary intervention (PCI) in native coronary arteries
- Treatment of de novo coronary artery lesions in vessels sized appropriately for a 3.00 mm device
- Use as part of a catheter-based revascularization workflow in the cardiac catheterization laboratory
- Suitability for specific lesion types and patient profiles must be determined by the treating physician per the current Instructions for Use
Product Information
- Brand: Abbott
- Product line: Xience Xpedition
- Category: Coronary Stents (drug-eluting)
- REF / UPN: 1070300-12
- Stent diameter: 3.00 mm
- Stent length: 12 mm
- Drug: Everolimus
- Stent material: Cobalt chromium alloy
- Delivery system: Rapid-exchange catheter
- Guidewire compatibility: Not specified in the located sources
- Guide catheter compatibility: Not specified in the located sources
- Rated burst pressure: Not specified in the located sources
- Sterilization: Sterile, single-use
- Storage: Refer to manufacturer IFU
- Regulatory status: Refer to local regulatory documentation and the current Abbott Instructions for Use
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