Firehawk Liberty 3.50 × 18 mm | REF FR3518

The MicroPort Firehawk Liberty (REF FR3518) is a drug-eluting coronary stent system with a nominal expanded diameter of 3.50 mm and a stent length of 18 mm. It is designed for percutaneous coronary intervention and is listed here for B2B procurement and catalog reference.

Key Features
Target-eluting technology with sirolimus carried in abluminal grooves of the stent struts.
Cobalt-chromium alloy stent platform intended to support a thin strut profile.
Rapid-exchange delivery catheter designed for navigation through the coronary vasculature.
Size configuration: 3.50 mm diameter × 18 mm length.
Additional coating, strut thickness, crossing profile and delivery system specifications: Not specified in the located sources.

Clinical Applications
Intended for use by trained interventional cardiologists in accordance with the manufacturer's Instructions for Use and applicable local regulatory clearances.
Indications, contraindications, warnings and precautions: refer to the official MicroPort Firehawk Liberty IFU. Specific approved indications are Not specified in the located sources.

Product Information
Brand: MicroPort
Product Line: Firehawk Liberty
Category: Coronary Stents
REF/UPN: FR3518
Diameter: 3.50 mm
Length: 18 mm
Sterility, shelf life and packaging details: Not specified in the located sources.

REF / UPNFR3518
Size18 mm

How It Works

1

Submit Your Request

Tell us what product you need and share a few details.

2

We Match You

We connect your request with the most relevant verified brands.

3

Receive Offers

Relevant supplier options can respond with availability, documentation context, and quote details.

Buyer support

Frequently asked questions about Firehawk Liberty 3.50 × 18 mm | REF FR3518

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.

Your request has been captured successfully.