
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 Terumo Ultimaster Nagomi Coronary Stent (REF DE-RQ3515KSM) is a sirolimus-eluting coronary stent system mounted on a rapid-exchange delivery catheter. This configuration provides a 3.50 mm expanded stent diameter and a 15 mm stent length, intended for percutaneous coronary intervention in adult patients. The Nagomi platform builds on the established Ultimaster family with a thin-strut cobalt-chromium scaffold and a bioresorbable abluminal polymer coating designed to support controlled drug release and early polymer clearance.
Key Features
- Sirolimus-eluting drug-eluting stent (DES) with bioresorbable abluminal PDLLA-PCL polymer coating
- Thin-strut cobalt-chromium alloy scaffold for deliverability and conformability
- Abluminal-only drug coating to limit luminal polymer exposure
- Rapid-exchange (monorail) delivery catheter with low crossing profile
- Radiopaque markers for fluoroscopic placement
- Expanded stent dimensions: 3.50 mm diameter × 15 mm length
- Supplied sterile, for single use only
Clinical Applications
- Percutaneous coronary intervention (PCI) in native coronary arteries
- Treatment of de novo coronary artery lesions in adult patients
- Use in catheterization laboratory and hybrid OR settings by trained interventional cardiologists
- Intended for procurement by hospitals, cardiac centers, and authorized B2B medical distributors
Product Information
- Brand: Terumo
- Product Line: Ultimaster Nagomi
- Category: Coronary Stents (Drug-Eluting)
- REF / UPN: DE-RQ3515KSM
- Stent Diameter: 3.50 mm
- Stent Length: 15 mm
- Drug: Sirolimus
- Polymer: Bioresorbable abluminal coating
- Scaffold Material: Cobalt-chromium alloy
- Delivery System: Rapid-exchange (monorail)
- 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
- Regulatory Status: Refer to local regulatory documentation and manufacturer IFU prior to clinical use
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