Thrombectomy devices
Triever24
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.
Triever24 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 |
|---|---|---|---|
| 22-101 | — | Not stated | Available |
FDA clearances
- 510(k) K213402 May 2022
Procedures that use thrombectomy devices
Frequently asked questions
What is Triever24 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 Triever24?
Triever24 is made by Inari Medical, Inc.. It is listed under mechanical thrombectomy devices in our device library.
What sizes does Triever24 come in?
The FDA device database does not list sizes for Triever24. Check the instructions for use or ask a Inari Medical, Inc. representative.
Is Triever24 MRI safe?
The FDA device database entry for Triever24 does not state its MRI safety status. Check the labeling before MRI.
Is Triever24 FDA cleared?
Triever24 is covered by FDA submission K213402.
How do I contact a Inari Medical, Inc. sales representative?
Inari Medical, Inc. has not listed representatives on LA Vascular yet. Visit the Inari Medical, 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.