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Cleaner Vac™

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Cleaner Vac™ FDA UDI
Generic Name
Thrombectomy suction catheter FDA UDI
Device Name
Cleaner Vac™ Aspiration Canister FDA UDI
Model / Reference
70020400 FDA UDI
Description
Cleaner Vac™ Aspiration Canister FDA UDI

Identifiers

Catalog Number
70020400 FDA UDI
Primary DI / UDI-DI
00886333227624 FDA UDI
510(k) Number
K232679 FDA UDI
FDA Product Code
QEW FDA UDI
KRA FDA UDI
GMDN Term
Thrombectomy suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5150 FDA UDI
870.1210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Thrombectomy suction catheter

Cleaner Vac™ by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy suction catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a2076a8-c42c-4edc-9b33-f30ae0e0faf8 37 fields · synced Jun 9, 2026