G-tubes

Corflo

by Corpak Medsystems, Inc.

A sterile, short, hollow tube that is inserted into the stomach percutaneously to permit long-term enteral feeding. The tube does not permit reflux and its external end is flush with abdominal skin. This is a single-use device.

Ask about this device Where to buy Compare similar devices

Where to buy Corflo

We do not have contact details for Corpak Medsystems, Inc. yet. Send a request and we will route it to the right person for your country.

Request this device

Is this your product? Claim Corpak Medsystems, Inc. to list your reps and distributors by country and receive buyer requests from your territories.

Corflo models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
31-5555— Not statedAvailable

Procedures that use g-tubes

Frequently asked questions

What is Corflo used for?

A sterile, short, hollow tube that is inserted into the stomach percutaneously to permit long-term enteral feeding. The tube does not permit reflux and its external end is flush with abdominal skin. This is a single-use device.

Who makes Corflo?

Corflo is made by Corpak Medsystems, Inc.. It is listed under gastrostomy and gj tubes in our device library.

What sizes does Corflo come in?

The FDA device database does not list sizes for Corflo. Check the instructions for use or ask a Corpak Medsystems, Inc. representative.

Is Corflo MRI safe?

The FDA device database entry for Corflo does not state its MRI safety status. Check the labeling before MRI.

Is Corflo FDA cleared?

Corflo is registered in the FDA's Global Unique Device Identification Database (GUDID).

How do I contact a Corpak Medsystems, Inc. sales representative?

Corpak Medsystems, Inc. has not listed representatives on LA Vascular yet. Visit the Corpak Medsystems, 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.

📬 The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you