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The Hydrophilic Guidewire is indicated for general intravascular use to aid in the selective placement of catheters in the peripheral and cerebral vasculature during diagnostic and/or therapeutic procedures. The device is not intended for use in the coronary arteries.
The Guidewire Torque Device is intended to facilitate guidewire manipulation during interventional procedures.
The Guidewire Introducer is intended to facilitate guidewire insertion into a catheter hub or through a hemostasis valve.
The .014” wire with distal polymer jacket is not DMSO compatible.
The guidewire is compatible with other ancillary products used in intravascular procedures. Any over-the-wire style of micro catheter used with the guidewire should have at least 0.0025” (0.06 mm) clearance between the lumen of catheter and the guidewire.
Procedures requiring percutaneous catheter introduction should not be attempted by physicians unfamiliar with the possible complications, which may occur during or after the procedure.
Possible complications include, but are not limited to, the following:
This device is intended for single use only. Discard the product after use. Structural integrity and/or function may be impaired through reuse or cleaning.
Never advance or withdraw the guidewire against resistance until the cause of the resistance is determined by fluoroscopy.
Do not attempt to move the guidewire without observing the resultant tip response.
See the device manual for detailed information regarding the instructions for use, indications, contraindications, warnings, precautions, and potential adverse events.
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