Uric Acid LiquiColor®

FDA UDI

Class I (US FDA UDI)

by Stanbio Laboratory, L.p.

Identity

Trade Name: Uric Acid LiquiColor® FDA UDI
Generic Name: Uric acid IVD, kit, spectrophotometry FDA UDI
Device Name: Quantitative Enzymatic Colorimetric Determination of Uric Acid in Serum, Plasma or Urine. FDA UDI
Model / Reference: 1045-225 FDA UDI
Description: Quantitative Enzymatic Colorimetric Determination of Uric Acid in Serum, Plasma or Urine. FDA UDI

Identifiers

Catalog Number: 1045-225 FDA UDI
Primary DI / UDI-DI: 00657498001110 FDA UDI
FDA Product Code: KNK FDA UDI
GMDN Term: Uric acid IVD, kit, spectrophotometry FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 862.1775 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Uric acid IVD, kit, spectrophotometry

Uric Acid LiquiColor® by Stanbio Laboratory, L.p. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Stanbio Laboratory, L.p.

Sources (1)

FDA UDI 0e0929f9-dea1-437e-a76f-0ba2ef50d47c 36 fields · synced May 30, 2026