
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 Elite Flow Diverter (REF FDE50015) is a self-expanding braided intracranial implant designed for the endovascular reconstruction of the parent artery in the treatment of intracranial aneurysms. With a labeled diameter of 5.0 mm and a working length of 15 mm, this device is intended to redirect blood flow away from the aneurysm sac while preserving flow through adjacent perforators and branches, promoting progressive aneurysm occlusion through intra-aneurysmal thrombosis and neointimal remodeling across the device.
Key Features
- Braided flow-diverting design engineered to provide consistent mesh density for hemodynamic flow disruption.
- Self-expanding construction for conformability to the parent vessel anatomy.
- Labeled dimensions: 5.0 mm nominal diameter x 15 mm working length.
- Pre-loaded delivery system intended for use with a compatible microcatheter (refer to manufacturer IFU for compatibility).
- Radiopaque markers to support fluoroscopic visualization during navigation, deployment, and post-deployment assessment.
- Single-use, sterile packaging.
Clinical Applications
- Endovascular treatment of intracranial aneurysms in appropriately selected parent vessels.
- Parent artery reconstruction in cerebrovascular interventional neuroradiology procedures.
- Use in neurovascular suites equipped for high-resolution biplane fluoroscopic imaging.
- Specific indications, contraindications, vessel diameter range, and patient selection criteria: Not specified in the located sources — refer to the current manufacturer Instructions for Use.
Product Information
- Brand: Stryker
- Product line: Surpass Elite Flow Diverter
- Reference / UPN: FDE50015
- Nominal diameter: 5.0 mm
- Working length: 15 mm
- Category: Flow Diverter / Neurovascular Implant
- Sterility: Sterile, single-use
- Delivery system / microcatheter compatibility: Not specified in the located sources
- Material composition: Not specified in the located sources
- Regulatory status: Not specified in the located sources — verify regional clearance prior to procurement.
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