Coils
Medusa Multi-Coil
A non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Medusa Multi-Coil 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 |
|---|---|---|---|
| MMC-120 | — | MR Conditional | Available |
| MMC-122 | — | MR Conditional | Available |
| MMC074-45 | — | MR Conditional | Available |
Procedures that use coils
Frequently asked questions
What is Medusa Multi-Coil used for?
A non-bioabsorbable, implantable device intended to induce a thrombosis within a non-neurovascular blood vessel to treat an aneurysm and/or non-neurovascular arteriovenous malformation (AVM); it is not intended for neurovascular application. It is in the form of a metal or metal/synthetic polymer wire which coils upon deployment within an aneurysm or the vasculature surrounding a malformation; it is typically pre-attached to a nonimplantable delivery wire. Disposable devices associated with implantation (e.g., delivery wire, catheter) may be included.
Who makes Medusa Multi-Coil?
Medusa Multi-Coil is made by Endoshape, Inc.. It is listed under embolization coils in our device library.
What sizes does Medusa Multi-Coil come in?
The FDA device database does not list sizes for Medusa Multi-Coil. Check the instructions for use or ask a Endoshape, Inc. representative.
Is Medusa Multi-Coil MRI safe?
The FDA device database lists Medusa Multi-Coil as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Medusa Multi-Coil FDA cleared?
Medusa Multi-Coil is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Endoshape, Inc. sales representative?
Endoshape, Inc. has not listed representatives on LA Vascular yet. Visit the Endoshape, 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.