Conventional Ports

AngioDynamics offers a complete line of conventional ports to meet your needs, including the LifePort®, TitanPort® and Triumph-1® models for which the specifications appear below.


The LifePort line of ports, complemented by the Bayonet locking mechanism, offers a complete line of venous ports, including a unique 6.6 French dual low profile model. A variety of sizes and catheter materials are available, along with both pre-attached and detached options.

  • Plastic and titanium models available
  • Silicone and polyurethane catheters available
  • Bayonet locking mechanism
  • Available in single, dual, low-profile, and dual low-profile models
  • Latex free
  • Titanium: MRI conditional – 3 Tesla/Single Lumen Plastic: MRI safe


The TitanPort line offers titanium models with silicone catheters.

  • Available in single models
  • Latex free/MRI conditional – 3 Tesla


The Triumph-1 vascular port features a complete line of single and low-profile ports that provide a 100 PSI rated silicone catheter.

  • Plastic and titanium models available
  • 100 PSI rated silicone catheters
  • One-step locking mechanism
  • Available in single and low profile models
  • Full placement kit
  • Latex free
  • Titanium & Plastic: MRI conditional – 3 Tesla


Important Risk Information

INDICATION FOR USE: AngioDynamics implantable access port systems are intended to facilitate frequent blood sampling or the delivery of medications, nutritions, blood products, and imaging solutions. CONTRAINDICATIONS: AngioDynamics port systems should not be implanted in the presence of known or suspected infections, septicemia, or peritonitis, in patients who have exhibited prior intolerance to the materials of construction, or patients whose body size or tissue is insufficient to accommodate the size of the port or catheter. CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician. WARNINGS AND PRECAUTIONS: The device is sterile and intended for single patient use. Sterile unless the package is opened or damaged. Do not re-sterilize. Use of AngioDynamics anti-coring (19 to 22 gauge Huber point) needles in all procedures is recommended. Observe all instructions for use. Failure to do so may result in patient complications or device damage. POTENTIAL COMPLICATIONS: Use of port systems involve potential risks normally associated with the insertion or use of any implanted device or indwelling catheter including but not limited to: Infection; pneumothorax; catheter malposition, migration or fragmentation; catheter pinch-off or rejection; hemorrhage; hematoma; clot formation, thrombophlebitis or thromboembolism; vessel trauma, including puncture, laceration, and erosion of vessel and skin; cardiac arrhythmia, puncture and tamponade; endocarditis; thoracic duct injury; peritonitis; fibrin sheath; and drug extravasation (leakage). Occlusion may result from clot formation inside the lumen of the catheter, precipitate formation inside the port from incompatible drugs, or from catheter tip placement against a vein wall or valve.

Indications, contraindications, warnings and instructions for use can be found in the instructions for use supplied with each device. Observe all instructions prior to use. Failure to do so may result in patient complications.