SPLIT CATH® Indications for Use: : The Medcomp® Pediatric Split Cath® XL is indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis and in pediatric, adolescent, and adult patients as determined by the prescribing physician. It may be inserted percutaneously and is primarily placed in the internal jugular vein. Alternate insertion sites include the subclavian and femoral vein. 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. SPLIT CATH® III Indications for Use: The Medcomp® Split Cath® III is indicated for use in attaining Long-Term vascular access for hemodialysis and apheresis in the adult population. It may be inserted percutaneously and is primarily placed in the internal jugular vein. Alternate insertion sites include the subclavian vein and inferior vena cava as required. Catheters greater than 40cm are intended for femoral vein or inferior vena cava insertion. Translumbar insertion via inferior vena cava is indicated when all other access sites are identified as non-viable. 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. SPLIT STREAM® Indications for Use: The Medcomp® Split Stream® is indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. It may be inserted percutaneously and is primarily placed in the internal jugular vein. Alternate insertion sites include the subclavian vein. Catheters greater than 40cm are intended for femoral vein insertion. 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. To maintain peak performance of the Split-Stream® extension set, it is recommended that the extension set be replaced every 6 months. TITAN HD Indications for Use: The Medcomp® Titan HD is indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. It may be inserted percutaneously and is primarily placed in the internal jugular vein of an adult patient. Alternate insertion sites includes the subclavian vein as required. 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-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 inserted percutaneously and is primarily placed in the internal jugular vein of an adult patient. Alternate insertion sites include subclavian vein as required. Catheters greater than 40cm are intended for femoral vein insertion. 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 inserted percutaneously and is primarily placed in the internal jugular vein of an adult patient. Alternate insertion sites include subclavian vein as required. The curved Hemo-Cath® Catheter is intended for internal jugular vein insertion. 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 inserted 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 insertion 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. Important Risk Information 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. For patient information please visit www.medcomp.net/patientinformation
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