Uric Acid Reagent 500mL
by Clinical Diagnostic Solutions, Inc.
Uric Acid Reagent 500mL (501-418) is a Class I device made by Clinical Diagnostic Solutions, Inc., listed in FDA GUDID since 12 Oct 2016 (UDI-DI 00812137012050), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00812137012050 | Date12 Oct 2016 | StatusListed |
Official records
- AccessGUDID record 00812137012050
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Uric Acid Reagent
- Generic name
- Uric acid IVD, reagent
- Model / Ref / Catalog
- 500mL, 501-418
- Primary DI / UDI-DI
- 00812137012050
- FDA product code
- KNK
- GMDN term
- Uric acid IVD, reagent
- Device class
- Class I
- Regulation number
- 862.1775
- GUDID distribution status
- In Commercial Distribution
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