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D-10

FDA UDI

Class II (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
D-10 FDA UDI
Generic Name
Glycated haemoglobin (HbA1c) IVD, kit, liquid chromatography FDA UDI
Device Name
D-10 Hemoglobin A1c Program FDA UDI
Model / Reference
12000949 FDA UDI
Description
D-10 Hemoglobin A1c Program FDA UDI

Identifiers

Catalog Number
12000949 FDA UDI
Primary DI / UDI-DI
03610520530108 FDA UDI
FDA Product Code
PDJ FDA UDI
GMDN Term
Glycated haemoglobin (HbA1c) IVD, kit, liquid chromatography FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1373 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Glycated haemoglobin (HbA1c) IVD, kit, liquid chromatography

D-10 by Bio-Rad Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glycated haemoglobin (HbA1c) IVD, kit, liquid chromatography.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3ab8f757-99e7-447f-b00b-676d76a4279e 36 fields · synced May 30, 2026