Neuro aspiration catheters

Cerenovus

by Cerenovus, Inc.

A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.

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Cerenovus models and sizes

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

Model / catalog no.SizeMRIStatus
EVT110Length 284 cm Not statedAvailable

FDA clearances

  • 510(k) K193380 July 2020

Procedures that use neuro aspiration catheters

Frequently asked questions

What is Cerenovus used for?

A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes (e.g., straight, hockey stick). It is not intended solely for infusion, is not intended to access superselective small vessels, and does not include a transseptal needle. It may include a disposable percutaneous introduction set or shaft visualization electrodes. This is a single-use device.

Who makes Cerenovus?

Cerenovus is made by Cerenovus, Inc.. It is listed under neurovascular aspiration catheters in our device library.

What sizes does Cerenovus come in?

Sizes listed for Cerenovus: Length: 284 cm. Confirm availability with the manufacturer's instructions for use.

Is Cerenovus MRI safe?

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

Is Cerenovus FDA cleared?

Cerenovus is covered by FDA submission K193380.

How do I contact a Cerenovus, Inc. sales representative?

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

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