Implanted ports
T-Port
A fully-implantable device assembly intended to provide access to arteries/veins (excludes coronary and intracerebral circulation) for infusion (e.g., chemotherapeutic agents, blood transfusions) and/or drainage (e.g., blood). It consists of: 1) a subcutaneous chamber, with a self-sealing puncturable septum for percutaneous insertion of a hypodermic needle; and 2) an attached catheter which passes into the arteries/veins. It may consist of two chambers attached to a dual-lumen catheter for simultaneous infusion. It is made of metal [e.g., titanium (Ti)] and/or synthetic polymers (e.g., silicone); disposable devices associated with implantation may be included.
Where to buy T-Port
We do not have contact details for Pfm Medical Incorporated yet. Send a request and we will route it to the right person for your country.
T-Port models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 611.366.2088-HA | — | Not stated | Available |
| 616.365.2080-A | — | Not stated | Available |
| 616.365.2081-A | — | Not stated | Available |
| 616.365.2087-HA | — | Not stated | Available |
| 616.365.2088-HA | — | Not stated | Available |
| 616.365.3078-HA | — | Not stated | Available |
| 616.366.2081-A | — | Not stated | Available |
| 616.366.2087-HA | — | Not stated | Available |
| 616.366.2088-HA | — | Not stated | Available |
| 616.366.3077-HA | — | Not stated | Available |
| 616.366.3078-HA | — | Not stated | Available |
| 616.465.1075-A | — | Not stated | Available |
FDA clearances
- 510(k) K073210 December 2007
Procedures that use implanted ports
Frequently asked questions
What is T-Port used for?
A fully-implantable device assembly intended to provide access to arteries/veins (excludes coronary and intracerebral circulation) for infusion (e.g., chemotherapeutic agents, blood transfusions) and/or drainage (e.g., blood). It consists of: 1) a subcutaneous chamber, with a self-sealing puncturable septum for percutaneous insertion of a hypodermic needle; and 2) an attached catheter which passes into the arteries/veins. It may consist of two chambers attached to a dual-lumen catheter for simultaneous infusion. It is made of metal [e.g., titanium (Ti)] and/or synthetic polymers (e.g., silicone); disposable devices associated with implantation may be included.
Who makes T-Port?
T-Port is made by Pfm Medical Incorporated. It is listed under implanted ports (port-a-cath) in our device library.
What sizes does T-Port come in?
The FDA device database does not list sizes for T-Port. Check the instructions for use or ask a Pfm Medical Incorporated representative.
Is T-Port MRI safe?
The FDA device database entry for T-Port does not state its MRI safety status. Check the labeling before MRI.
Is T-Port FDA cleared?
T-Port is covered by FDA submission K073210.
How do I contact a Pfm Medical Incorporated sales representative?
Pfm Medical Incorporated has not listed representatives on LA Vascular yet. Visit the Pfm Medical Incorporated company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.