
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-RS3515ASM) is a sirolimus-eluting coronary stent system mounted on a rapid-exchange delivery catheter, configured at 3.50 mm diameter and 15 mm length. The Ultimaster Nagomi platform builds on the Ultimaster family and combines a thin-strut cobalt-chromium scaffold with an abluminal bioresorbable PDLLA-PCL polymer carrier designed to elute sirolimus and then resorb, leaving a polymer-free metal stent.
Key Features
Thin-strut cobalt-chromium stent platform engineered for deliverability and conformability.
Abluminal-only bioresorbable polymer (PDLLA-PCL) coating for controlled, gradient drug release.
Sirolimus as the active pharmaceutical agent.
Rapid-exchange (monorail) delivery catheter compatible with standard PCI workflows.
Stent size: 3.50 mm × 15 mm; reference code DE-RS3515ASM.
Clinical Applications
Intended for percutaneous coronary intervention in adult patients with ischemic heart disease, including treatment of de novo coronary artery lesions. Suitable diameter and length selection should be based on operator assessment, vessel sizing and lesion characteristics. Specific indications, contraindications, warnings and precautions are defined by the manufacturer Instructions for Use and applicable regional approvals.
Product Information
Brand: Terumo
Product line: Ultimaster Nagomi
Category: Coronary Stents (Drug-Eluting)
REF / UPN: DE-RS3515ASM
Stent diameter: 3.50 mm
Stent length: 15 mm
Drug: Sirolimus
Polymer: Bioresorbable PDLLA-PCL, abluminal coating
Stent material: Cobalt-chromium alloy
Delivery system: Rapid-exchange (monorail)
Guide wire compatibility: Not specified in the located sources
Guiding catheter compatibility: Not specified in the located sources
Sterilization: Not specified in the located sources
Single use: Not specified in the located sources
Regulatory status: Refer to the manufacturer Instructions for Use for region-specific approvals.
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