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BUN Reagent, Liquid

FDA UDI

Class I (US FDA UDI)

by Cliniqa Corporation

Identity

Trade Name
BUN Reagent, Liquid FDA UDI
Generic Name
Urea IVD, reagent FDA UDI
Device Name
BUN Reagent, Liquid FDA UDI
Model / Reference
R84533 FDA UDI
Description
BUN Reagent, Liquid FDA UDI

Identifiers

Primary DI / UDI-DI
00817238011193 FDA UDI
510(k) Number
K012649 FDA UDI
FDA Product Code
CDG FDA UDI
GMDN Term
Urea IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1385 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: Urea IVD, reagent

BUN Reagent, Liquid by Cliniqa Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urea IVD, reagent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cliniqa Corporation

Sources (1)

  • FDA UDI e50f3cad-3aa9-48b0-834f-69152d145132 34 fields · synced May 30, 2026