Guidewires
Impella
A sterile tubular device with a built-in electrically-powered axial flow pump (e.g., a micro motor with an impeller) at the distal end, designed to provide circulatory assistance to the heart by pumping blood during heart failure. It is inserted through the lumen of the aorta and into the left ventricle, surgically or percutaneously via an artery, and connected to an external control unit; it moves blood from the left ventricle to the aorta across the aortic valve. It is typically used emergently post acute myocardial infarction (AMI), electively for high-risk cardiac catheterization, for open chest surgery, and during transport between hospitals. This is a single-use device.
Impella 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 |
|---|---|---|---|
| 0052-3005 | — | Not stated | Available |
| 0052-3018 | — | Not stated | Available |
Procedures that use guidewires
Frequently asked questions
What is Impella used for?
A sterile tubular device with a built-in electrically-powered axial flow pump (e.g., a micro motor with an impeller) at the distal end, designed to provide circulatory assistance to the heart by pumping blood during heart failure. It is inserted through the lumen of the aorta and into the left ventricle, surgically or percutaneously via an artery, and connected to an external control unit; it moves blood from the left ventricle to the aorta across the aortic valve. It is typically used emergently post acute myocardial infarction (AMI), electively for high-risk cardiac catheterization, for open chest surgery, and during transport between hospitals. This is a single-use device.
Who makes Impella?
Impella is made by Abiomed, Inc.. It is listed under guidewires in our device library.
What sizes does Impella come in?
The FDA device database does not list sizes for Impella. Check the instructions for use or ask a Abiomed, Inc. representative.
Is Impella MRI safe?
The FDA device database entry for Impella does not state its MRI safety status. Check the labeling before MRI.
Is Impella FDA cleared?
Impella is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Abiomed, Inc. sales representative?
Abiomed, Inc. has not listed representatives on LA Vascular yet. Visit the Abiomed, 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.