Implanted ports
Dignitypower Injectable Titanium 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.
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Where to buy Dignitypower Injectable Titanium Port
Contact Medical Components, Inc. directly; they can quote, ship, or point you to the distributor for your country.
From medcomp.net, checked October 2026.
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Dignitypower Injectable Titanium 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 |
|---|---|---|---|
| MITTI66041M | — | MR Conditional | Available |
| MRTTI50041 | — | MR Conditional | Available |
| MRTTI50841 | — | MR Conditional | Available |
| MRTTI50841M | — | MR Conditional | Available |
| MRTTI66041 | — | MR Conditional | Available |
| MRTTI66041M | — | MR Conditional | Available |
| MRTTI80001 | — | MR Conditional | Available |
| MRTTI80041 | — | MR Conditional | Available |
| MRTTI80041M | — | MR Conditional | Available |
| MRTTI80801 | — | MR Conditional | Available |
| MRTTI80841 | — | MR Conditional | Available |
| MRTTI96001 | — | MR Conditional | Available |
| MRTTI96801 | — | MR Conditional | Available |
Procedures that use implanted ports
Frequently asked questions
What is Dignitypower Injectable Titanium 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 Dignitypower Injectable Titanium Port?
Dignitypower Injectable Titanium Port is made by Medical Components, Inc.. It is listed under implanted ports (port-a-cath) in our device library.
What sizes does Dignitypower Injectable Titanium Port come in?
The FDA device database does not list sizes for Dignitypower Injectable Titanium Port. Check the instructions for use or ask a Medical Components, Inc. representative.
Is Dignitypower Injectable Titanium Port MRI safe?
The FDA device database lists Dignitypower Injectable Titanium Port as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Dignitypower Injectable Titanium Port FDA cleared?
Dignitypower Injectable Titanium Port is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Medical Components, Inc. sales representative?
Medical Components, Inc. has not listed representatives on LA Vascular yet. Visit the Medical Components, Inc. 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.