LONG TERM HEMODIALYSIS CATHETERS Split Cath® Split Cath® III Split Stream® Tesio® Titan HD Hemo-Flow® Hemo-Cath® LT Symetrex® Repair Kit HEMO-FLOW® Indications for Use: The Hemo-Flow® Catheter is indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. It may be inser ted percutaneously and is primarily placed in the internal jugular vein of an adult patient. Alternate inser tion sites include subclavian vein as required. Catheters greater than 40cm are intended for femoral vein inser tion. Contraindications: This catheter is intended for Long-Term vascular access only and should not be used for any purpose other than indicated in these instructions. HEMO-CATH® LT Indications for Use: The Hemo-Cath® Dialysis Catheter is indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. It may be inser ted percutaneously and is primarily placed in the internal jugular vein of an adult patient. Alternate inser tion sites include subclavian vein as required. The curved Hemo-Cath® Catheter is intended for internal jugular vein inser tion. Contraindications: This catheter is intended for Long-Term vascular access only and should not be used for any purpose other than indicated in these instructions. SYMETREX® Indications for Use: The Symetrex® Long Term Hemodialysis Catheter is a symmetric tip dual lumen catheter designed for chronic hemodialysis and apheresis. It may be inser ted percutaneously or by cut down. Catheters with greater than 37 cm implant length are indicated for femoral placement. Contraindications: Do not use this catheter in thrombosed vessels or for subclavian puncture when ventilator is in use. This device is contraindicated whenever: Used for any purpose other than indicated in these instructions. The presence of other device related infection, or septicemia is known or suspected. Injection caps are not intended to be punctured with a needle. Severe chronic obstructive lung disease is present. Tissue factors in the localized area of device placement will prevent proper device stabilization and/or access. Venous thrombosis or vascular surgical procedures have occurred at the prospective placement site. Post irradiation of prospective inser tion site. MEDCOMP® REPAIR KIT Indications for Use: To replace damaged female luer connectors, clamps, or repair extensions where there is a minimum of 4.5cm viable extension tubing. Contraindications: Do not use to repair catheters other than those specified above. Do not replace connector if tubing is swollen or displays signs of degradation. This repair kit should not be used for any purpose other than indicated in these instructions. TESIO® REPAIR KIT Indications for Use: The Medcomp® Tesio® Catheter is designed for Long Term Hemodialysis and Apheresis. It may be inser ted percutaneously, and is ideally placed in the internal jugular vein. Although this catheter may be inser ted into the subclavian vein, the internal jugular vein is the preferred site. Contraindications: This extension is not intended for any use other than that which is indicated. To maintain peak performance of the extension, it is recommended that the extensions be replaced every 6 months. Refer to Instructions for Use provided with the product for complete instructions, warnings, and contraindications. Observe all instructions for use prior to using products. Failure to do so may result in patient complications. Long Term
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