Exodus Array Multipurpose Drainage Catheters are intended for percutaneous drainage of fluid or air in the chest, abdomen and pelvis, e.g., abscesses, cysts, pneumothoraces, biliary, nephrostomy, urinary, pleural, empyemas, lung abscesses and mediastinal collections.
Exodus Nuance Nephrostomy Drainage Catheters are intended for percutaneous drainage of fluid collections on the urinary system. Exodus Believe Biliary Drainage Catheters are intended for percutaneous drainage of the biliary tree.
CONTRAINDICATIONS: Bleeding diathesis and anticoagulant use.
WARNING: Contents supplied STERILE using an ethylene oxide (EO) process. Do not use if sterile barrier is damaged. If damage is found, call your sales representative. Inspect prior to use to verify that no damage has occurred during shipping. For single patient use only. Do not reuse, reprocess or resterilize. Reuse, reprocessing or resterilization may compromise the structural integrity of the device and/ or lead to device failure which, in turn, may result in patient injury, illness or death. Reuse, reprocessing or resterilization may also create a risk of contamination of the device and/or cause patient infection or cross-infection, including, but not limited to, the transmission of infectious disease(s) from one patient to another. Contamination of the device may lead to injury, illness or death of the patient.
After use, dispose of product and packaging in accordance with hospital, administrative and/or local government policy.
• Do not use catheter for gastrostomy procedures/ feeding tube. Exposure to gastric juices may damage the catheter.
• Do not place catheter into the vascular system.
• Do not expose this catheter to alcohol, as it may damage the hydrophilic coating and the catheter.
• The Exodus Drainage Catheters have not been evaluated for safety and compatibility in the MR environment. They have not been tested for heating, migration, or image artifact in the MR environment. The safety of Exodus Drainage Catheters in the MR environment is unknown. Scanning a patient who has this device may result in patient injury.
• There is a potential risk of misconnections with connectors from other healthcare applications, such as intravenous equipment, breathing and driving gas systems, urethral/urinary, limb cuff inflation neuraxial devices and other enteral and gastric applications.
Refer to Directions for use provided with the product for complete instructions, warnings and precautions/ cautions.
CAUTION: Federal Law (USA) restricts this device to sale by or on the order of a physician.
