Verify

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name: VERIFY FDA UDI
Generic Name: Biological sterilization indicator FDA UDI
Device Name: The VERIFY V24 Challenge Pack is for qualifications testing of the V-PRO Low Temperature Sterilization Systems following installation, relocation, malfunctions or major repairs. FDA UDI
Model / Reference: LCB005 FDA UDI
Description: The VERIFY V24 Challenge Pack is for qualifications testing of the V-PRO Low Temperature Sterilization Systems following installation, relocation, malfunctions or major repairs. FDA UDI

Identifiers

Catalog Number: LCB005 FDA UDI
Primary DI / UDI-DI: 10724995180291 FDA UDI
510(k) Number: K073618 FDA UDI
K090514 FDA UDI
K092906 FDA UDI
K103331 FDA UDI
K140499 FDA UDI
K172748 FDA UDI
K183300 FDA UDI
FDA Product Code: FRC FDA UDI
JOJ FDA UDI
GMDN Term: Biological sterilization indicator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.2800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Biological sterilization indicator

Verify by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K090514 also covers:

VERIFY — STERIS CORPORATION

K140499 also covers:

VERIFY — STERIS CORPORATION

K172748 also covers:

VERIFY — STERIS CORPORATION

K183300 also covers:

VERIFY — STERIS CORPORATION

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: Steris Corporation

Sources (1)

FDA UDI 6c82c86f-ecaa-40d7-96a6-a09b2306e0a0 37 fields · synced Jun 8, 2026