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Liquichek

FDA UDI

Class I (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
Liquichek FDA UDI
Generic Name
Glycated haemoglobin (HbA1c) IVD, control FDA UDI
Device Name
Liquichek Diabetes Control Level Trilevel MiniPak (A human whole blood assayed diabetes control.) FDA UDI
Model / Reference
12011331 FDA UDI
Description
Liquichek Diabetes Control Level Trilevel MiniPak (A human whole blood assayed diabetes control.) FDA UDI

Identifiers

Catalog Number
12011331 FDA UDI
Primary DI / UDI-DI
03610522142415 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Glycated haemoglobin (HbA1c) 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glycated haemoglobin (HbA1c) IVD, control

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

Similar devices

Also classified as Glycated haemoglobin (HbA1c) IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e6ce1211-471e-4bae-baed-84d9c0cb36d4 36 fields · synced May 30, 2026