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Liquichek 12011331

by Bio-Rad Laboratories

Liquichek 12011331 is a Class I device made by Bio-Rad Laboratories, listed in FDA GUDID since 27 Aug 2021 (UDI-DI 03610522142415), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03610522142415 UDI-DI Date27 Aug 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Liquichek
Generic name
Glycated haemoglobin (HbA1c) IVD, control
Model / Ref / Catalog
12011331
Primary DI / UDI-DI
03610522142415
FDA product code
JJX
GMDN term
Glycated haemoglobin (HbA1c) IVD, control
Device class
Class I
Regulation number
862.1660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Glycated haemoglobin (HbA1c) IVD, control

Similar devices in this category

Other devices filed under Glycated haemoglobin (HbA1c) IVD, control.

Other devices from Bio-Rad Laboratories

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)