
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 MicroPort Firehawk (REF RV2708) is a targeted drug-eluting coronary stent system in a 2.75 mm x 8 mm size configuration, supplied for B2B procurement by hospitals, cath labs and authorized medical distributors. The Firehawk platform is designed by MicroPort Scientific to deliver an anti-proliferative agent from abluminal grooves on the stent surface, supporting controlled drug release in coronary applications.
Key Features
- Brand: MicroPort
- Product family: Firehawk targeted drug-eluting coronary stent
- Reference / UPN: RV2708
- Nominal stent diameter: 2.75 mm
- Nominal stent length: 8 mm
- Stent platform material: cobalt-chromium alloy
- Drug coating: sirolimus released from abluminal grooves with a biodegradable polymer carrier
- Delivery system: rapid-exchange (Rx) balloon catheter
- Sterility: supplied sterile, single-use device
Clinical Applications
- Intended for use in percutaneous coronary intervention (PCI) procedures.
- Suitable size range for treatment of de novo coronary artery lesions where a 2.75 mm vessel diameter and 8 mm lesion length are appropriate, as determined by the treating physician.
- Used in interventional cardiology cath lab settings.
- Final patient selection, indications, contraindications and procedural use must follow the official MicroPort Firehawk Instructions For Use and applicable local regulatory labeling.
Product Information
- Manufacturer: MicroPort Scientific Corporation
- Category: Coronary Stents / Drug-Eluting Stents
- REF / UPN: RV2708
- Configuration: 2.75 mm diameter x 8 mm length, mounted on rapid-exchange delivery catheter
- Guide wire compatibility: Not specified in the located sources
- Minimum guide catheter inner diameter: Not specified in the located sources
- Rated burst pressure and nominal pressure: Not specified in the located sources
- Shelf life: Not specified in the located sources
- Regulatory clearance status: varies by market; buyers must verify approval and availability in their jurisdiction 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.