
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 Firebird 2 Coronary Stent (REF G3521) is a sirolimus-eluting coronary stent system with a nominal expanded diameter of 3.50 mm and a stent length of 21 mm, pre-mounted on a rapid-exchange delivery catheter. The Firebird 2 platform is built on a cobalt-chromium alloy stent scaffold combined with a sirolimus drug-polymer coating intended to support controlled antiproliferative drug release during the post-implantation period.
Key Features
Cobalt-chromium alloy stent platform designed for thin strut geometry and radial support.
Sirolimus drug coating paired with a carrier polymer for sustained antiproliferative elution.
Pre-mounted on a rapid-exchange (monorail) balloon delivery catheter for single-operator use.
Radiopaque balloon markers to assist fluoroscopic positioning during deployment.
Nominal stent dimensions 3.50 mm x 21 mm as identified by reference code G3521.
Individually packaged sterile, single-use device intended for one-time deployment.
Clinical Applications
Supplied for use in percutaneous coronary intervention (PCI) procurement programs within cardiac catheterization laboratories.
Intended for catalog listing alongside other drug-eluting stent (DES) sizes used in the treatment of coronary artery lesions.
Commonly specified for hospital cath lab inventory, interventional cardiology case carts, and tender or group purchasing organization (GPO) submissions.
Final clinical selection, lesion suitability, sizing and implantation technique remain the responsibility of the treating interventional cardiologist.
Product Information
Brand: MicroPort
Product Line: Firebird 2 Sirolimus-Eluting Coronary Stent System
Category: Coronary Stents / Drug-Eluting Stents
REF / UPN: G3521
Stent Diameter: 3.50 mm
Stent Length: 21 mm
Stent Material: Cobalt-chromium alloy
Active Drug: Sirolimus
Delivery System: Rapid-exchange balloon catheter
Usable Catheter Length: Not specified in the located sources
Guidewire Compatibility: Not specified in the located sources
Minimum Guiding Catheter ID: Not specified in the located sources
Nominal / Rated Burst Pressure: Not specified in the located sources
Sterilization: Sterile, single-use
Regulatory Status: Refer to local regulatory documentation and the manufacturer IFU for market-specific clearances.
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