F18H15ST300

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Indications, Safety, and WarningsIndications (or Intended Use)FMD Peripheral Guide Wires are intended to facilitate the placement and exchange of diagnostic and therapeutic devices during intravascular procedures. This device is intended for peripheral use only.ContraindicationsThis guide wire is not intended for use in coronary or cerebral vasculatures and not intended for use with atherectomy devices.Potential Adverse Events (or Potential Complications)Possible complications and adverse events of guide wire use include, but are not limited to: Access site complications, Allergic reaction (to contrast, device or other), Aneurysm, Angina or unstable angina, Bleeding / hemorrhage, Bradycardia / Palpitation, Cardiac tamponade / pericardial effusion, Death, Embolization (plaque, thrombus, device, tissue, or other), Fistula of artery or vein, Hypotension / Hypertension, Infection, Myocardial infarction or ischemia, Separation or breakage of the guide wire, Stroke / cerebral vascular accident (CVA) / transient ischemic attack (TIA), Thrombosis / Thrombus, Vasospasm, Vessel trauma / perforation / dissection, X-Ray radiation exposure complications (e.g., alopecia, burns ranging in severity from skin reddening to ulcers, cataracts, and delayed neoplasia).CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician. Important Information: Indications, contraindications, warnings and instructions for use can be found in the product labeling supplied with each device.UC202501855 EN

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Find more information, including other available configurations, for F-14™* and F-18™* peripheral guidewires.

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