
Synergy Shield Coronary Stent 2.25 X 8 | REF H7493966608220
Boston Scientific Synergy Shield Coronary Stent, 2.25 mm x 8 mm, REF H7493966608220. Single-unit B2B catalog listing for hospital and cath lab procurement.

The Terumo Ultimaster Nagomi Coronary Stent (REF DE-RS3038ASM) is a sirolimus-eluting coronary stent system with a nominal expanded diameter of 3.00 mm and a stent length of 38 mm. It is designed for use during percutaneous coronary intervention (PCI) procedures and combines a thin-strut cobalt-chromium platform with a bioresorbable abluminal polymer coating that releases sirolimus.
Key Features
- Thin-strut cobalt-chromium stent platform engineered for deliverability and conformability.
- Abluminal-only bioresorbable PDLLA-PCL polymer coating designed to elute sirolimus and resorb over time.
- Sirolimus drug coating intended to support controlled antiproliferative release.
- Premounted on a rapid-exchange (Rx) delivery catheter for monorail technique.
- Stent length: 38 mm; nominal diameter: 3.00 mm.
- Reference / UPN: DE-RS3038ASM.
Clinical Applications
- Intended for use in percutaneous coronary intervention to improve coronary luminal diameter.
- Suitable workhorse sizing for de novo lesions in native coronary arteries within the labeled vessel diameter range.
- Compatible with standard PCI workflows including direct stenting and post-dilatation per operator technique.
- Specific indications, contraindications, warnings and patient selection criteria: refer to the official Terumo Instructions for Use (IFU).
Product Information
- Brand: Terumo
- Product line: Ultimaster Nagomi
- Category: Coronary Stents (drug-eluting)
- Drug: Sirolimus
- Polymer: Bioresorbable abluminal coating
- Stent material: Cobalt-chromium alloy
- Delivery system: Rapid-exchange (monorail)
- Diameter × Length: 3.00 mm × 38 mm
- REF / UPN: DE-RS3038ASM
- Guidewire compatibility, crossing profile, recommended guide catheter ID, nominal/RBP pressures and shelf life: Not specified in the located sources — refer to the manufacturer specification sheet and IFU.
- Sterility, single-use status and storage conditions: refer to product labeling.
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.