24 Fr Evacuation System

FDA UDI

Class II (US FDA UDI)

by Inari Medical, Inc.

Identity

Trade Name: 24 Fr Evacuation System FDA UDI
Generic Name: Thrombectomy suction catheter FDA UDI
Device Name: 24 Fr Evacuation System FDA UDI
Model / Reference: 131-102 / AS-01229 FDA UDI
Description: 24 Fr Evacuation System FDA UDI

Identifiers

Primary DI / UDI-DI: 00810123710485 FDA UDI
510(k) Number: K233069 FDA UDI
FDA Product Code: PUR FDA UDI
GMDN Term: Thrombectomy suction catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5860 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

Category: Thrombectomy suction catheter

24 Fr Evacuation System by Inari Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy suction catheter.

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Prodigy™ Catheter — IMPERATIVE CARE INC. · Class II
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Indigo System — PENUMBRA, INC. · Class II
Penumbra System — PENUMBRA, INC. · Class II
Trevo — Stryker Corp.
Penumbra System — PENUMBRA, INC. · Class II
Pounce ™ Thrombectomy — Surmodics, Inc. · Class II

Cleared under the same submission

K233069 also covers:

16 Fr Evacuation System — Inari Medical, Inc.

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: Inari Medical, Inc.

Sources (1)

FDA UDI bfea244c-d268-4b80-9dca-1391fd89ccb6 35 fields · synced May 30, 2026