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Liquid Glycated Haemoglobin (HbA1c) Control Level 1 (LIQ HbA1c CONTROL LEVEL 1)

FDA UDI

Class I (US FDA UDI)

by Randox Laboratories, Ltd.

Identity

Trade Name
Liquid Glycated Haemoglobin (HbA1c) Control Level 1 (LIQ HbA1c CONTROL LEVEL 1) FDA UDI
Generic Name
Glycated haemoglobin (HbA1c) IVD, control FDA UDI
Device Name
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems. FDA UDI
Model / Reference
HA10224 FDA UDI
Description
This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems. FDA UDI

Identifiers

Catalog Number
HA10224 FDA UDI
Primary DI / UDI-DI
05055273215656 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Liquid Glycated Haemoglobin (HbA1c) Control Level 1 (LIQ HbA1c CONTROL LEVEL 1) by Randox Laboratories, Ltd. — Class I — FDA UDI — listed in FDA GUDID

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 81d3b7b5-1ab6-44d0-b7c1-54c724ff2bf0 36 fields · synced Jun 6, 2026