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Verify

FDA UDI

Class I (US FDA UDI)

by Albert Browne , Ltd.

Identity

Trade Name
VERIFY FDA UDI
Generic Name
Chemical/physical sterilization process indicator FDA UDI
Device Name
VERIFY DualAction Ultrasonic Indicator is intended to verify the ultrasonic activity and performance of ultrasonic cleaners operating in the frequency range of 38 - 40kHz. FDA UDI
Model / Reference
LCC027 FDA UDI
Description
VERIFY DualAction Ultrasonic Indicator is intended to verify the ultrasonic activity and performance of ultrasonic cleaners operating in the frequency range of 38 - 40kHz. FDA UDI

Identifiers

Catalog Number
LCC027 FDA UDI
Primary DI / UDI-DI
10724995231887 FDA UDI
FDA Product Code
FLG FDA UDI
GMDN Term
Chemical/physical sterilization process indicator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Chemical/physical sterilization process indicator

Verify by Albert Browne , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chemical/physical sterilization process indicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Albert Browne , Ltd.

Sources (1)

  • FDA UDI aaec2121-1632-4ad4-ac35-c447cfba850a 35 fields · synced Jun 7, 2026