
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 Stryker Surpass Evolve Flow Diverter (REF FD40030) is a self-expanding, braided flow-diverting stent designed for endovascular reconstruction of the parent artery in the treatment of intracranial aneurysms. This configuration is supplied in a 4.00 mm nominal vessel diameter by 30 mm working length and is delivered through a compatible microcatheter using an integrated delivery system.
Key Features
- Braided multi-wire construction using cobalt-chromium and platinum-tungsten wires for radial support and fluoroscopic visibility.
- 64-wire braid design intended to provide consistent metal coverage and pore density across the labeled diameter range.
- Self-expanding with resheathing capability prior to final detachment to support repositioning during deployment.
- Radiopaque markers on the implant and delivery wire to aid placement under fluoroscopy.
- Pre-loaded delivery system compatible with standard 0.027 inch inner diameter microcatheters (verify against current IFU).
- Sterile, single-use packaging.
Clinical Applications
- Endovascular treatment of intracranial aneurysms via parent-vessel reconstruction.
- Use in large or giant wide-necked aneurysms where flow diversion is the selected strategy by the treating neurointerventionalist.
- Suitable for target vessels within the labeled 4.00 mm diameter range; refer to the manufacturer IFU for vessel sizing, anatomy, and patient selection criteria.
- Intended for use by physicians trained in interventional neuroradiology and flow-diverter implantation techniques.
Product Information
- Brand: Stryker Neurovascular
- Product line: Surpass Evolve Flow Diverter
- REF / UPN: FD40030
- Nominal vessel diameter: 4.00 mm
- Implant length: 30 mm
- Category: Flow Diverter / Neurovascular Implant
- Material: Cobalt-chromium and platinum-tungsten braided wires
- Delivery system compatibility: Not specified in the located sources — verify with current IFU
- Sterility: Sterile, single-use
- Regulatory status: Not specified in the located sources — confirm regional clearance 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.