Pro-PICC® Vascu-PICC® Vascu-PICC® TL Vascu-PICC® TLS Valved Pro-PICC® Valved Vascu-PICC® PERIPHERALLY INSERTED CENTRAL CATHETERS IMPORTANT RISK INFORMATION PRO-PICC® Indications for Use: The Pro-PICC® CT catheter is indicated for shor t 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. 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 inser tion 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® / VASCU-PICC® TL Indications for Use: The Peripherally Inser ted Central Vein Access Catheters are designed for Long or Shor t- Term peripheral access to the central venous system for intravenous therapy and blood sampling, and allows for central venous pressure monitoring. 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. VASCU-PICC® TLS Indications for Use: The 1.9F and 2.6F Peripherally Inser ted Central Vein Access Catheters are indicated for shor t or long term access to the central venous system via peripheral inser tion in neonates, infants, and children. It may be used for administration of fluids, medication, and nutritional therapy. Recommended inser tion sites are the median cubital vein of the elbow or the basilic vein. The long saphenous veins of the ankle may also be used. This catheter is not suitable for inser tion through non-superficial veins. 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. 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. VALVED PRO-PICC® Indications for Use: The Pro-PICC® CT catheter with valve technology is indicated for shor t 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. 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 inser tion 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. 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. PICCs
RkJQdWJsaXNoZXIy MTYyNDM3Mw==