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Liquichek

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
Liquichek FDA UDI
Generic Name
Multiple clinical chemistry protein IVD, control FDA UDI
Device Name
Liquichek Specialty Immunoassay Plus Control Level 3 (A human serum assayed immunoassay control.) FDA UDI
Model / Reference
12015647 FDA UDI
Description
Liquichek Specialty Immunoassay Plus Control Level 3 (A human serum assayed immunoassay control.) FDA UDI

Identifiers

Catalog Number
12015647 FDA UDI
Primary DI / UDI-DI
03610522231102 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple clinical chemistry protein 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple clinical chemistry protein IVD, control

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

Similar devices

Also classified as Multiple clinical chemistry protein IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ba8b65cc-904e-449c-9c38-80bde9410a25 36 fields · synced Jun 8, 2026