Aventus Thrombectomy System - Clot Management System

FDA UDI

Class II (US FDA UDI)

by Inquis Medical, Inc.

Identity

Trade Name: Aventus Thrombectomy System - Clot Management System FDA UDI
Generic Name: Thrombectomy suction catheter FDA UDI
Device Name: The Aventus Clot Management System is connected to the aspiration syringe and is used to filter and return blood to the patient as desired. The clot canister contains a coarse pre-filter to separate blood from clot and is designed to be compatible with off-the-shelf blood transfusion filters. FDA UDI
Model / Reference: IM-0002 FDA UDI
Description: The Aventus Clot Management System is connected to the aspiration syringe and is used to filter and return blood to the patient as desired. The clot canister contains a coarse pre-filter to separate blood from clot and is designed to be compatible with off-the-shelf blood transfusion filters. FDA UDI

Identifiers

Catalog Number: CMS-M FDA UDI
Primary DI / UDI-DI: 00860009303416 FDA UDI
510(k) Number: K240426 FDA UDI
FDA Product Code: CAC FDA UDI
GMDN Term: Thrombectomy suction catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5830 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Thrombectomy suction catheter

Aventus Thrombectomy System - Clot Management System by Inquis Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Inquis Medical, Inc.

Sources (1)

FDA UDI 58df160a-07fd-41cb-859a-ae4a4396eed8 36 fields · synced May 30, 2026