PERIPHERALLY INSERTED CENTRAL CATHETERS Pro-PICC® Vascu-PICC® Vascu-PICC® TL Vascu-PICC® TLS Valved Pro-PICC® VASCU-PICC® TLS Indications for Use: The 1.9F Vascu-PICC® is a long-term catheter intended for central venous access via peripheral insertion in neonates, infants and children. It may be used for administration of fluids, medication and nutritional therapy. Indications for Use: The 2.6F Vascu-PICC® catheters are indicated for short or long term access to the central venous system via peripheral insertion in neonates, infants and children. It may be used for the administration of fluids, medication and nutritional therapy. 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. 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. VALVED PRO-PICC® Indications for Use: The Pro-PICC® CT catheter with valve technology is indicated for short 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 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. 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. 50 PICCs
RkJQdWJsaXNoZXIy MTYyNDM3Mw==