IMPORTANT RISK INFORMATION PRO-PICC® Indications for Use: The Pro-PICC® CT catheter is indicated for short term or long term peripheral access to the central venous system for intravenous therapy and power injection of contrast media, and allows for central venous pressure monitoring, when a 20 gauge or larger lumen is used. For blood sampling, infusion, or therapies, use a 4F or larger catheter. The maximum recommended infusion rate varies by catheter French size and is printed on the catheter. (3 French) Indications for Use: The 3F Pro-PICC® CT catheter is indicated for short term or long term peripheral access to the central venous system for intravenous therapy and power injection of contrast media, and allows for central venous pressure monitoring. The maximum recommended infusion rate varies by catheter French size and is printed on the catheter. (6 French Triple-Full Nursing and Max Barrier) Indications for Use: The Pro-PICC® CT catheter is indicated for short term or long term peripheral access to the central venous system for intravenous therapy and power injection of contrast media. For blood sampling, infusion, or therapies, use a 4F or larger catheter. The maximum recommended infusion rate varies by catheter French size and is printed on the catheter. Contraindications: The presence of device related infection, bacteremia, or septicemia is known or suspected. 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. There has been past irradiation of prospective insertion site. There have been previous episodes of venous thrombosis or vascular surgical procedures at the prospective placement site. There are local tissue factors that may prevent proper device stabilization and/or access. VASCU-PICC® Indications for Use: The Peripherally Inserted Central Vein Access catheters are designed for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling. For central venous pressure monitoring (CVP), it is recommended that catheter lumen of 20 gauge or larger be used. 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 insertion site (infection, phlebitis, scars, etc.) The presence of device related bacteremia or septicemia. History of mastectomy on insertion side. Previous history of venous/subclavian thrombosis or vascular surgical procedures at insertion 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 insertion site. Local tissue factors will prevent proper device stabilization and/or access. VASCU-PICC® TL Indications for Use: The Peripherally Inserted Central Vein Access catheters are designed for long- or short-term peripheral access to the central venous system for intravenous therapy and blood sampling and allows for central venous pressure monitoring. (MR81014106MB & MR81015206MB) Indications for Use: The Peripherally Inserted Central Vein Access catheters are designed for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling. For central venous pressure monitoring (CVP), it is recommended that catheter lumen of 20 gauge or larger be used. 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 insertion site (infection, phlebitis, scars, etc.) The presence of device related bacteremia or septicemia. History of mastectomy on insertion side. Previous history of venous/subclavian thrombosis or vascular surgical procedures at insertion 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 insertion site. Local tissue factors will prevent proper device stabilization and/or access.
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