Stryker Trevo Pro 18 Microcatheter | REF 90238

The Stryker Trevo Pro 18 Microcatheter (REF 90238) is a single-lumen, variable-stiffness neurovascular microcatheter engineered for selective access into the distal cerebral vasculature. It is intended to support controlled delivery and deployment of compatible neurovascular devices, including the Trevo Retriever family of stentrievers, during interventional neurovascular procedures.

Key Features
Single-lumen microcatheter platform from Stryker Neurovascular.
Variable-stiffness shaft design intended to balance proximal pushability with distal flexibility.
Lubricious hydrophilic coating on the distal segment to support tracking through tortuous anatomy.
Distal radiopaque marker(s) to assist fluoroscopic visualization during navigation and device deployment.
Configured for use with compatible 0.014 in class guidewires; refer to the manufacturer IFU for exact compatibility.
Intended to accommodate Trevo Retriever stentrievers and other compatible neurovascular devices per IFU.

Clinical Applications
Selective and super-selective catheterization of the neurovasculature.
Delivery vehicle for compatible stent retrievers in mechanical thrombectomy workflows.
Controlled introduction of diagnostic contrast media or compatible therapeutic agents into the cerebral vessels.
Procedural support during interventional neuroradiology cases involving distal cerebral access.

Product Information
Brand: Stryker (Stryker Neurovascular)
Product: Trevo Pro 18 Microcatheter
REF / UPN: 90238
Category: Neurovascular Microcatheters
Lumen: Single lumen
Inner Diameter: Not specified in the located sources
Outer Diameter (distal): Not specified in the located sources
Working Length: Not specified in the located sources
Guidewire Compatibility: 0.014 in class guidewires per IFU; refer to manufacturer documentation
Coating: Hydrophilic distal coating
Sterility: Supplied sterile, single-use device
Packaging: Not specified in the located sources
Regulatory: Refer to current manufacturer IFU and regional regulatory documentation for approved indications and use.

REF / UPN90238
Size

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