
FRED Junior System 2.5 | REF FREDJR2508
Terumo Neuro FRED Junior System 2.5 (REF FREDJR2508) is a low-profile dual-layer flow diverter designed for the endovascular treatment of intracranial aneurysms in smaller parent vessels.

The Terumo Neuro FRED System 3.5 (REF FRED3536) is a dual-layer flow diverter designed for the endovascular treatment of intracranial aneurysms. The device combines an outer low-porosity stent with an inner high-porosity braid in a single delivery system, intended to redirect blood flow away from the aneurysm sac while supporting parent artery reconstruction.
Key Features
Dual-layer braided design integrating flow-diverting inner mesh and outer stent scaffold.
Self-expanding nitinol construction with tantalum radiopaque markers for fluoroscopic visibility.
Pre-loaded on a single delivery wire for controlled deployment and partial resheathing prior to detachment.
Nominal labeled diameter 3.5 mm; working length and vessel sizing per manufacturer instructions for use.
Designed for navigation through standard neurovascular microcatheters compatible with the FRED System (refer to current IFU for compatibility).
Clinical Applications
Endovascular flow diversion of intracranial aneurysms in selected parent arteries.
Reconstruction of the parent vessel in wide-neck, large, or complex aneurysm morphologies.
Use within the labeled vessel diameter and indication range as defined by the manufacturer's instructions for use and applicable regional regulatory clearance.
Product Information
Brand: Terumo Neuro
Product: FRED System 3.5
REF / UPN: FRED3536
Category: Flow Diverter (Neurovascular)
Device Diameter: 3.5 mm (nominal)
Device Length: Not specified in the located sources
Material: Nitinol braid with tantalum radiopaque markers
Delivery: Pre-loaded single-wire delivery system
Sterility: Supplied sterile, single use (refer to IFU)
Storage and Handling: Per manufacturer IFU
Always consult the current manufacturer Instructions for Use for indications, contraindications, sizing matrix, microcatheter compatibility, and regional regulatory status prior to use.
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.