Stent retrievers

Embotrap

by Neuravi Limited

A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.

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Where to buy Embotrap

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Embotrap models and sizes

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

Model / catalog no.SizeMRIStatus
ET009521β€” Not statedAvailable
ET009533β€” Not statedAvailable
ET309522β€” Not statedAvailable
ET309537β€” Not statedAvailable
ET309645β€” Not statedAvailable

FDA clearances

  • 510(k) K251789 September 2025
  • 510(k) K211338 July 2021
  • 510(k) K193063 July 2020
  • 510(k) K173452 May 2018

Procedures that use stent retrievers

Frequently asked questions

What is Embotrap used for?

A flexible or semi-flexible tube designed for the percutaneous, transluminal disruption and removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction in native/stented blood vessels, native/synthetic bypass grafts, and/or haemodialysis access grafts, through suction (aspiration) in conjunction with a syringe or dedicated suction pump system (pump not included). It may additionally be intended for infusion of fluids and/or used as a guide-catheter to facilitate introduction of a thrombectomy wire-net (not included) to remove residual thrombus. Collection containers may be included with the catheter. This is a single-use device.

Who makes Embotrap?

Embotrap is made by Neuravi Limited. It is listed under stent retrievers for stroke in our device library.

What sizes does Embotrap come in?

The FDA device database does not list sizes for Embotrap. Check the instructions for use or ask a Neuravi Limited representative.

Is Embotrap MRI safe?

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

Is Embotrap FDA cleared?

Embotrap is covered by FDA submissions K173452, K193063, K251789, K211338.

How do I contact a Neuravi Limited sales representative?

Neuravi Limited has not listed representatives on LA Vascular yet. Visit the Neuravi Limited 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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