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Verify

FDA UDI

Class II (US FDA UDI)

by Albert Browne , Ltd.

Identity

Trade Name
VERIFY FDA UDI
Generic Name
Medical device disinfection solution test strip FDA UDI
Device Name
The VERIFY Chemical Indicator for S40 Sterilant is a peracetic acid concentration indicator for routine monitoring of the System 1E Liquid Chemical Sterilant Processing System employing S40 Sterilant Concentrate. FDA UDI
Model / Reference
LCC016 FDA UDI
Description
The VERIFY Chemical Indicator for S40 Sterilant is a peracetic acid concentration indicator for routine monitoring of the System 1E Liquid Chemical Sterilant Processing System employing S40 Sterilant Concentrate. FDA UDI

Identifiers

Catalog Number
LCC016 FDA UDI
Primary DI / UDI-DI
10724995162600 FDA UDI
510(k) Number
K102217 FDA UDI
K173428 FDA UDI
FDA Product Code
JOJ FDA UDI
GMDN Term
Medical device disinfection solution test strip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Cleared under the same submission

K102217 also covers:

K173428 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2bf062bd-e19e-42e7-a513-d571f6754cb3 38 fields · synced May 29, 2026