
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-RS3018ASM) is a sirolimus-eluting coronary stent system designed for percutaneous coronary intervention. The 3.00 × 18 mm size is mounted on a rapid-exchange delivery catheter intended to facilitate navigation through tortuous coronary anatomy and precise lesion coverage.
Key Features
- Drug: Sirolimus elution from a bioresorbable abluminal polymer coating (PDLLA-PCL)
- Stent platform: Thin-strut cobalt-chromium scaffold
- Nominal diameter: 3.00 mm
- Stent length: 18 mm
- Delivery system: Rapid-exchange (monorail) over 0.014" guidewire
- Coating distribution: Abluminal-only to support controlled drug release
- Radiopaque markers for fluoroscopic placement
- Sterile, single-use device
Clinical Applications
- Percutaneous coronary intervention in patients with symptomatic ischemic heart disease
- Treatment of de novo coronary artery lesions in vessels suited to a 3.00 mm reference diameter
- Use within indications, contraindications and warnings stated in the manufacturer Instructions For Use
Product Information
- Brand: Terumo
- Product line: Ultimaster Nagomi
- Category: Coronary Stents (Drug-Eluting)
- REF / UPN: DE-RS3018ASM
- Size: 3.00 mm × 18 mm
- Guidewire compatibility: 0.014"
- Guiding catheter compatibility: Not specified in the located sources
- Crossing profile: Not specified in the located sources
- Rated burst pressure: Not specified in the located sources
- Sterilization: Sterile, single-use; refer to IFU
- Storage and handling: Per manufacturer IFU
Tell us what product you need and share a few details.
We connect your request with the most relevant verified brands.
Relevant supplier options can respond with availability, documentation context, and quote details.
Practical answers for procurement teams reviewing this product page.
Include the exact product family, brand preference, REF/UPN code when available, required quantity, destination country, expected delivery timing and documentation expectations.
Yes. If alternatives are acceptable, mention equivalent brands, compatible models, size ranges and any non-negotiable requirements.
Related products are connected through structured catalog data such as brand, category, product family and country assignment.
No. This page supports sourcing and RFQ organization. Buyers must verify regulatory status, clinical suitability and procurement compliance independently.
Specific codes reduce ambiguity and help supplier teams identify product availability, packaging details and documentation faster.
Yes. The workflow is designed for hospitals, clinics, distributors, wholesalers, importers and procurement departments.
Yes. Products can be connected to multiple countries in the admin panel, and buyers can specify destination details in the RFQ form.
The request is stored with contact and procurement details so the sourcing conversation can be reviewed and followed up clearly.