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ADVIA® Chemistry UA Uric Acid Reagents

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA® Chemistry UA Uric Acid Reagents FDA UDI
Generic Name
Uric acid IVD, kit, spectrophotometry FDA UDI
Device Name
Uric Acid - ADVIA Chem. - RGT - 7x140 tests FDA UDI
Model / Reference
10309492 FDA UDI
Description
Uric Acid - ADVIA Chem. - RGT - 7x140 tests FDA UDI

Identifiers

Catalog Number
7497014 FDA UDI
Primary DI / UDI-DI
00630414508313 FDA UDI
510(k) Number
K991576 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

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, kit, spectrophotometry

ADVIA® Chemistry UA Uric Acid Reagents by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uric acid IVD, kit, spectrophotometry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 45a41b65-2eb6-49dc-a34c-d4a97a803366 37 fields · synced May 30, 2026