← Back to catalogue

Verify

FDA UDI

Class II (US FDA UDI)

by Steris Corporation

Identity

Trade Name
VERIFY FDA UDI
Generic Name
Chemical/physical sterilization process indicator FDA UDI
Device Name
The VERIFY All-In-One Steam Reusable Test Pack with Tracker Tag is designed to challenge vacuum assisted steam sterilizers operating at 270°F for a 4-minute exposure and can be used 200 times. FDA UDI
Model / Reference
LCB057 FDA UDI
Description
The VERIFY All-In-One Steam Reusable Test Pack with Tracker Tag is designed to challenge vacuum assisted steam sterilizers operating at 270°F for a 4-minute exposure and can be used 200 times. FDA UDI

Identifiers

Catalog Number
LCB057 FDA UDI
Primary DI / UDI-DI
00724995162795 FDA UDI
FDA Product Code
FRC FDA UDI
GMDN Term
Chemical/physical sterilization process 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Chemical/physical sterilization process indicator

Verify by Steris Corporation — Class II — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI f22bbd02-6c0c-4b14-89fb-c81d714239fc 35 fields · synced Jun 8, 2026