
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 Abbott Xience Pro A Coronary Stent (REF 1128275-15) is a single-use, sterile drug-eluting coronary stent system with a nominal expanded diameter of 2.75 mm and a stent length of 15 mm. It is part of Abbott's Xience family of everolimus-eluting coronary stents, pre-mounted on a rapid-exchange delivery catheter for use during percutaneous coronary intervention (PCI).
Key Features
- Drug coating: Everolimus-eluting on a cobalt chromium stent platform
- Stent diameter: 2.75 mm nominal expanded diameter
- Stent length: 15 mm
- Delivery system: Rapid-exchange (monorail) balloon catheter
- Platform: Thin-strut cobalt chromium alloy with conformable design
- Polymer: Fluorinated biocompatible polymer carrier
- Packaging: Sterile, single-use, pre-mounted stent system
- Guidewire compatibility: Not specified in the located sources
Clinical Applications
- Intended for use in percutaneous coronary intervention procedures
- Suitable vessel reference diameter range and lesion length indications: Refer to the official Instructions for Use
- Used by interventional cardiology teams in cardiac catheterization laboratories
- Specific patient selection, contraindications and anti-platelet regimen: Not specified in the located sources
Product Information
- Brand: Abbott
- Product line: Xience Pro A
- Category: Coronary Stents
- REF / UPN: 1128275-15
- Stent size: 2.75 mm x 15 mm
- Sterility: Sterile, single-use device
- Storage and shelf life: Not specified in the located sources
- Regulatory clearances: Not specified in the located sources; buyers should confirm local regulatory status prior to procurement
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.