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Variant Ii Turbo

FDA UDI

Class II (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
VARIANT II TURBO FDA UDI
Generic Name
Glycated haemoglobin (HbA1c) IVD, kit, liquid chromatography FDA UDI
Device Name
VARIANT II TURBO HbA1c Kit - 2.0 FDA UDI
Model / Reference
12000447 FDA UDI
Description
VARIANT II TURBO HbA1c Kit - 2.0 FDA UDI

Identifiers

Catalog Number
12000447 FDA UDI
Primary DI / UDI-DI
03610520506547 FDA UDI
FDA Product Code
JKA FDA UDI
PDJ FDA UDI
GMDN Term
Glycated haemoglobin (HbA1c) IVD, kit, liquid chromatography FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
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

Yes

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

Variant Ii Turbo 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 1ab16ff1-37e6-446e-a9a8-322b89625937 36 fields · synced Jun 6, 2026