CT Midline Arch-Flo™ CT Midline MIDLINE IMPORTANT RISK INFORMATION CT MIDLINE Indications for Use: The CT Midlines are indicated for Shor t-Term peripheral access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media. The maximum recommended infusion rate varies by catheter French size and is printed on the catheter. Contraindications: This catheter is not intended for any use other than that which is indicated. Do not implant catheter in thrombosed vessels. The presence of skin related problems around the inser tion site (infection, phlebitis, scars, etc.). The presence of device related bacteremia or septicemia. History of mastectomy on inser tion side. Previous history of venous/subclavian thrombosis or vascular surgical procedures at inser tion site. Fever of unknown origin. The patient's body size is insufficient to accommodate the size of the implanted device. The patient is known or is suspected to be allergic to materials contained in the device. Past irradiation of prospective inser tion site. Local tissue factors will prevent proper device stabilization and/or access. ARCH-FLO™ CT MIDLINE Indications for Use: The Arch-Flo™ CT Midline is indicated for Shor t-Term, less than 30 days, peripheral access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media. This catheter may be inser ted via the basilic, cephalic, or median cubital vein. Contraindications: This catheter is not intended for any use other than that which is indicated. Do not implant catheter in thrombosed vessels. The presence of skin related problems around the inser tion site (infection, phlebitis, scars, etc.). The presence of device related bacteremia or septicemia. History of mastectomy on inser tion side. Previous history of venous/subclavian thrombosis or vascular surgical procedures at inser tion site. Fever of unknown origin. The patient's body size is insufficient to accommodate the size of the implanted device. The patient is known or is suspected to be allergic to materials contained in the device. Past irradiation of prospective inser tion site. Local tissue factors will prevent proper device stabilization and/or access. Refer to Instructions for Use provided with the product for complete instructions, warnings, precautions, and contraindications. Observe all instructions for use prior to using products. Failure to do so may result in patient complications. Midline
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