
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-RS2521ASM) is a sirolimus-eluting coronary stent system with a nominal expanded diameter of 2.50 mm and a stent length of 21 mm, supplied pre-mounted on a rapid-exchange percutaneous transluminal coronary angioplasty (PTCA) delivery catheter. It is designed to support vessel patency following balloon dilatation in patients undergoing percutaneous coronary intervention.
Key Features
- Thin-strut cobalt-chromium platform engineered for deliverability and conformability in tortuous coronary anatomy.
- Bioresorbable polymer drug coating abluminally applied, releasing sirolimus as the antiproliferative agent.
- Rapid-exchange (monorail) delivery system compatible with standard 0.014" guidewires.
- Low crossing profile intended to facilitate access to distal and small-vessel lesions.
- Radiopaque markers on the delivery balloon to aid fluoroscopic positioning.
- Pre-mounted, single-use, sterile configuration for procedural efficiency.
Clinical Applications
- Percutaneous coronary intervention in native coronary arteries.
- Treatment of small-diameter coronary vessels where a 2.50 mm device is appropriate.
- Use in mid-length lesions suitable for a 21 mm stent.
- Cath-lab inventory for interventional cardiology programs requiring a range of drug-eluting stent sizes. Clinical suitability for any individual patient must be determined by the treating physician in accordance with the manufacturer's Instructions for Use.
Product Information
- Brand: Terumo
- Product line: Ultimaster Nagomi
- Category: Coronary Stents (Drug-Eluting)
- REF / UPN: DE-RS2521ASM
- Nominal stent diameter: 2.50 mm
- Stent length: 21 mm
- Drug: Sirolimus
- Polymer: Bioresorbable, abluminal coating
- Delivery system: Rapid-exchange PTCA catheter
- Guidewire compatibility: 0.014"
- Packaging: Single-use, sterile, pre-mounted
- Guide catheter compatibility: Not specified in the located sources
- Rated burst pressure: Not specified in the located sources
- Shelf life: Not specified in the located sources
- Regulatory status: Refer to local regulatory labeling and the manufacturer's Instructions for Use.
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