
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 Boston Scientific Promus Elite Coronary Stent (REF H7493941328270) is a coronary stent device offered in a 2.75 mm diameter by 28 mm length configuration. This catalog listing is intended for qualified B2B medical device procurement and supply chain professionals.
Key Features
- Brand: Boston Scientific
- Product line: Promus Elite
- Diameter: 2.75 mm
- Length: 28 mm
- REF/UPN: H7493941328270
- Category: Coronary Stents
Clinical Applications
Coronary stents in this category are generally associated with percutaneous coronary intervention procedures. Specific indications, contraindications, and clinical suitability are Not specified in available product context and must be confirmed against the manufacturer's current Instructions for Use.
Product Information
- Manufacturer: Boston Scientific
- Reference number: H7493941328270
- Configuration: 2.75 x 28 mm
- Packaging: Not specified in available product context
- Sterility: Not specified in available product context
- Shelf life / expiration: Not specified in available product context
- Regulatory status: Not specified in available product context
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.