
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 Xience Pro S Coronary Stent by Abbott (REF 1508300-15) is a drug-eluting coronary stent system in a 3.00 mm × 15 mm configuration, designed for use in percutaneous coronary intervention procedures. It belongs to Abbott's established Xience family of everolimus-eluting coronary stents used by interventional cardiology teams.
Key Features
Everolimus drug-eluting coronary stent platform
Nominal diameter: 3.00 mm
Stent length: 15 mm
Pre-mounted on a rapid-exchange delivery catheter
Cobalt chromium stent platform per Xience family design
Sterile, single-use device
Clinical Applications
Intended for use by trained interventional cardiologists in percutaneous coronary intervention
Treatment of de novo coronary artery lesions in suitable patients
Supports revascularization workflows in cardiac catheterization laboratories
Specific indications, contraindications and patient selection criteria: refer to the manufacturer Instructions for Use
Product Information
Brand: Abbott
Product: Xience Pro S Coronary Stent
REF / UPN: 1508300-15
Diameter: 3.00 mm
Length: 15 mm
Category: Coronary Stents
Drug coating: Everolimus-eluting (per Xience platform)
Sterility: Sterile, single-use
Storage and shelf life: Not specified in the located sources
Regulatory status: Not specified in the located sources — refer to the manufacturer IFU and local regulatory documentation
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.