
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-RS2044ASM) is a sirolimus-eluting coronary stent system supplied in a 2.00 mm x 44 mm configuration. Pre-mounted on a rapid-exchange delivery catheter, it is designed to support percutaneous coronary intervention (PCI) workflows where lesion access, deliverability, and controlled drug elution are required.
Key Features
Sirolimus-eluting coronary stent platform from the Ultimaster Nagomi family.
Cobalt-chromium thin-strut stent architecture for conformability and trackability.
Bioresorbable polymer coating engineered for abluminal drug release.
Pre-mounted on a low-profile rapid-exchange (Rx) delivery catheter.
Long 44 mm working length suited to extended or tandem lesion segments.
Small 2.00 mm nominal diameter for distal and small-vessel anatomy.
Single-use, sterile packaged device with unique REF DE-RS2044ASM identifier.
Clinical Applications
Intended for use in percutaneous coronary intervention to improve coronary luminal diameter.
Applicable in patients with symptomatic ischemic heart disease due to de novo lesions in native coronary arteries, in line with the manufacturer's Instructions for Use.
Length and diameter selected to address long lesions in small-caliber coronary vessels.
Use is restricted to trained interventional cardiologists in catheterization laboratory settings.
Product Information
Brand: Terumo
Product Line: Ultimaster Nagomi
Category: Coronary Stents (Drug-Eluting)
REF / UPN: DE-RS2044ASM
Stent Diameter: 2.00 mm
Stent Length: 44 mm
Drug Coating: Sirolimus with bioresorbable polymer
Delivery System: Rapid-exchange (Rx) catheter, pre-mounted
Stent Material: Cobalt-chromium alloy
Sterility: Sterile, single-use
Guide Wire Compatibility: Not specified in the located sources
Guide Catheter Compatibility: Not specified in the located sources
Regulatory Status: Refer to local regulatory clearance and manufacturer IFU prior to use.
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