Nephrostomy catheters

Kaye

by Cook Incorporated

A sterile, flexible tube with an inflatable balloon at its distal end intended to be inserted into the uterus and distended with a medium (e.g., sterile water, medical air or other appropriate gas) to reduce postpartum bleeding with pressure. It may have an additional balloon inflated in the upper vagina to seal the uterine cavity. Devices associated with balloon inflation may be included. This is a single-use device.

Contact Cook Incorporated ↗ Where to buy Compare similar devices

Find similar drainage catheters

Where to buy Kaye

Contact Cook Incorporated directly; they can quote, ship, or point you to the distributor for your country.

From cookmedical.com, 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.

Is this your product? Claim Cook Incorporated to list your reps and distributors by country and receive buyer requests from your territories.

Kaye models and sizes

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

Model / catalog no.SizeMRIStatus
G14343— Not statedAvailable
G14423— Not statedAvailable

Procedures that use nephrostomy catheters

Frequently asked questions

What is Kaye used for?

A sterile, flexible tube with an inflatable balloon at its distal end intended to be inserted into the uterus and distended with a medium (e.g., sterile water, medical air or other appropriate gas) to reduce postpartum bleeding with pressure. It may have an additional balloon inflated in the upper vagina to seal the uterine cavity. Devices associated with balloon inflation may be included. This is a single-use device.

Who makes Kaye?

Kaye is made by Cook Incorporated. It is listed under nephrostomy and nephroureteral catheters in our device library.

What sizes does Kaye come in?

The FDA device database does not list sizes for Kaye. Check the instructions for use or ask a Cook Incorporated representative.

Is Kaye MRI safe?

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

Is Kaye FDA cleared?

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

How do I contact a Cook Incorporated sales representative?

Cook Incorporated has not listed representatives on LA Vascular yet. Visit the Cook 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.

📬 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