← Back to catalogue

Uric Acid Reagent

FDA UDI

Class I (US FDA UDI)

by Clinical Diagnostic Solutions, Inc.

Identity

Trade Name
Uric Acid Reagent FDA UDI
Generic Name
Uric acid IVD, reagent FDA UDI
Device Name
For the quantitative determination of Uric Acid in serum. For in vitro diagnostic use only. The determination of uric acid in serum is most commonly performed for the diagnosis of gout. Increased uric acid levels are also found in leukemia, polycythemia, familial idiopathic hyperuricemia, and conditions associated with decreased renal function. FDA UDI
Model / Reference
500mL FDA UDI
Description
For the quantitative determination of Uric Acid in serum. For in vitro diagnostic use only. The determination of uric acid in serum is most commonly performed for the diagnosis of gout. Increased uric acid levels are also found in leukemia, polycythemia, familial idiopathic hyperuricemia, and conditions associated with decreased renal function. FDA UDI

Identifiers

Catalog Number
501-418 FDA UDI
Primary DI / UDI-DI
00812137012050 FDA UDI
FDA Product Code
KNK FDA UDI
GMDN Term
Uric acid IVD, reagent 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

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

No

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

Category: Uric acid IVD, reagent

Uric Acid Reagent by Clinical Diagnostic Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uric acid IVD, reagent.

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

Sources (1)

  • FDA UDI b88337ce-f3a8-4957-ae2c-d692d35c2b8a 36 fields · synced May 31, 2026