Embolic beads
Gel-Bead
A bioabsorbable preformed device made from animal-derived (e.g., porcine) materials intended to be implanted in a non-neurovascular blood vessel, permanently or long-term, to occlude blood flow typically for treatment of an aneurysm, tumour (e.g., nephroma, hepatoma, uterine fibroids), and/or arteriovenous malformation (AVM). It is typically in the form of a gelatin foam pledget and may be supplied with dedicated instruments for implantation. This device is not intended to be used in intracranial arteries or for other neurovascular applications.
Gel-Bead 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 |
|---|---|---|---|
| IPN001479 | — | Not stated | Available |
| IPN001481 | — | Not stated | Available |
| IPN001483 | — | Not stated | Available |
| IPN001485 | — | Not stated | Available |
Procedures that use embolic beads
Frequently asked questions
What is Gel-Bead used for?
A bioabsorbable preformed device made from animal-derived (e.g., porcine) materials intended to be implanted in a non-neurovascular blood vessel, permanently or long-term, to occlude blood flow typically for treatment of an aneurysm, tumour (e.g., nephroma, hepatoma, uterine fibroids), and/or arteriovenous malformation (AVM). It is typically in the form of a gelatin foam pledget and may be supplied with dedicated instruments for implantation. This device is not intended to be used in intracranial arteries or for other neurovascular applications.
Who makes Gel-Bead?
Gel-Bead is made by Teleflex Incorporated. It is listed under embolic microspheres and particles (beads) in our device library.
What sizes does Gel-Bead come in?
The FDA device database does not list sizes for Gel-Bead. Check the instructions for use or ask a Teleflex Incorporated representative.
Is Gel-Bead MRI safe?
The FDA device database entry for Gel-Bead does not state its MRI safety status. Check the labeling before MRI.
Is Gel-Bead FDA cleared?
Gel-Bead is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Teleflex Incorporated sales representative?
Teleflex Incorporated has not listed representatives on LA Vascular yet. Visit the Teleflex 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.