Firebird 2 Coronary Stent 2.50 × 31 mm | REF G2531

The MicroPort Firebird 2 Coronary Stent (REF G2531) is a sirolimus-eluting coronary stent system with a nominal diameter of 2.50 mm and a stent length of 31 mm. It is supplied pre-mounted on a rapid-exchange delivery catheter and is intended for use by trained interventional cardiology professionals in qualified catheterization facilities. This listing is provided for B2B medical device procurement and catalog reference purposes only.

Key Features
Sirolimus-eluting coronary stent platform designed for percutaneous coronary intervention.
Nominal stent diameter: 2.50 mm.
Nominal stent length: 31 mm.
Pre-mounted on a rapid-exchange (monorail) delivery system.
Stent material, strut thickness, and polymer composition: Not specified in the located sources.
Nominal and rated burst pressures: Not specified in the located sources.
Guide wire and guide catheter compatibility: Not specified in the located sources.

Clinical Applications
Intended for use in interventional cardiology procedures involving coronary artery lesions, as determined by the treating clinician in accordance with the manufacturer's Instructions for Use.
Specific indications, contraindications, warnings, and precautions: Refer to the official MicroPort Firebird 2 Instructions for Use.
Regulatory clearances and approved markets: Not specified in the located sources; purchasers must verify local regulatory status prior to procurement.

Product Information
Brand: MicroPort
Product: Firebird 2 Coronary Stent
REF / UPN: G2531
Diameter: 2.50 mm
Length: 31 mm
Category: Coronary Stents
Drug coating: Sirolimus
Delivery system: Rapid-exchange catheter
Sterility / shelf life / packaging configuration: Not specified in the located sources.

REF / UPNG2531
Size31 mm
Buyer support

Frequently asked questions about Firebird 2 Coronary Stent 2.50 × 31 mm | REF G2531

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.