
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 MicroPort Firehawk Rapamycin Target Eluting Coronary Stent System (REF RV3516, 3.50 mm × 16 mm) is a cobalt-chromium coronary stent featuring abluminal grooves that carry a biodegradable polymer with sirolimus (rapamycin). The targeted abluminal coating is designed to deliver the drug toward the vessel wall while minimizing total polymer and drug load, mounted on a low-profile rapid exchange (Rx) delivery catheter for use during percutaneous coronary intervention (PCI).
Key Features
- Targeted drug elution: Sirolimus carried within abluminal grooves for vessel-wall directed release.
- Biodegradable polymer: PDLLA-based carrier designed to resorb after drug release.
- Low drug and polymer load: Engineered to reduce total polymer and drug exposure compared with conventional DES coatings.
- Cobalt-chromium platform: Thin-strut scaffold for deliverability and radial support.
- Rapid exchange delivery system: Rx catheter for single-operator handling over a 0.014" guidewire.
- Radiopaque markers: Two markers on the delivery balloon to aid stent positioning.
Clinical Applications
- Percutaneous coronary intervention in patients with symptomatic ischemic heart disease due to de novo native coronary artery lesions.
- Treatment of vessels with a reference diameter compatible with the 3.50 mm stent size.
- Use in catheterization laboratories performing PCI procedures with appropriate guide catheter and 0.014" guidewire support.
Product Information
- Brand: MicroPort
- Product: Firehawk Rapamycin Target Eluting Coronary Stent System
- REF / UPN: RV3516
- Stent diameter: 3.50 mm
- Stent length: 16 mm
- Stent material: Cobalt-chromium alloy
- Drug: Sirolimus (rapamycin)
- Polymer: Biodegradable, abluminal groove coating
- Delivery system: Rapid exchange (Rx), 0.014" guidewire compatible
- Category: Coronary Stents
- Sterility and shelf life: Not specified in the located sources
- Guide catheter compatibility: Not specified in the located sources
- Regulatory status: Refer to the manufacturer Instructions for Use for region-specific approvals.
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