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Liquichek

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
Liquichek FDA UDI
Generic Name
Microalbumin IVD, control FDA UDI
Device Name
Liquichek Microalbumin Control Level 2 (A human urine assayed chemistry control.) FDA UDI
Model / Reference
379 FDA UDI
Description
Liquichek Microalbumin Control Level 2 (A human urine assayed chemistry control.) FDA UDI

Identifiers

Catalog Number
379 FDA UDI
Primary DI / UDI-DI
00847661003434 FDA UDI
510(k) Number
K072835 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Microalbumin IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Microalbumin IVD, controlCreatinine IVD, control

Liquichek by Bio-Rad Laboratories — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Creatinine IVD, control.

Cleared under the same submission

K072835 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio-Rad Laboratories

Sources (1)

  • FDA UDI c4d4ba27-2a2d-4a49-b905-b80b5ad1315c 37 fields · synced Jun 6, 2026