Implanted ports
Pro-Fuse
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 Pro-Fuse
Contact Medical Components, Inc. directly; they can quote, ship, or point you to the distributor for your country.
From medcomp.net, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
Pro-Fuse 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 |
|---|---|---|---|
| MIPP50ALN | — | MR Conditional | Available |
| MIPP50ALS | — | MR Conditional | Available |
| MIPP50PLN | — | MR Conditional | Available |
| MIPP50PLS | — | MR Conditional | Available |
| MIPP66ALN | — | MR Conditional | Available |
| MIPP66ALS | — | MR Conditional | Available |
| MIPP66PLN | — | MR Conditional | Available |
| MIPP66PLS | — | MR Conditional | Available |
| MIPP80AFS | — | MR Conditional | Available |
| MIPP80ALN | — | MR Conditional | Available |
| MIPP80ALS | — | MR Conditional | Available |
| MIPP80PFS | — | MR Conditional | Available |
| MIPP80PLN | — | MR Conditional | Available |
| MIPP80PLS | — | MR Conditional | Available |
| MIPP96AFS | — | MR Conditional | Available |
| MIPP96PFS | — | MR Conditional | Available |
| MRCTI80001OR | — | MR Conditional | Available |
| MRCTT80001OR | — | MR Conditional | Available |
| MRPP80ALS | — | MR Conditional | Available |
| MRPP80ALS | — | MR Conditional | Available |
| MRPP80PFS | — | MR Conditional | Available |
| MRPP80PFS | — | MR Conditional | Available |
| MRPP80PLN | — | MR Conditional | Available |
| MRPP80PLS | — | MR Conditional | Available |
| MRPP80PLS | — | MR Conditional | Available |
| MRPP96AFS | — | MR Conditional | Available |
| MRPP96AFS | — | MR Conditional | Available |
| MRPP96PFS | — | MR Conditional | Available |
Procedures that use implanted ports
Frequently asked questions
What is Pro-Fuse 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 Pro-Fuse?
Pro-Fuse is made by Medical Components, Inc.. It is listed under implanted ports (port-a-cath) in our device library.
What sizes does Pro-Fuse come in?
The FDA device database does not list sizes for Pro-Fuse. Check the instructions for use or ask a Medical Components, Inc. representative.
Is Pro-Fuse MRI safe?
The FDA device database lists Pro-Fuse as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Pro-Fuse FDA cleared?
Pro-Fuse 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.