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VARIANT II Hemoglobin A1c

FDA UDI

Class II (US FDA UDI)

by Bio-Rad Laboratories

Identity

Trade Name
VARIANT II Hemoglobin A1c FDA UDI
Generic Name
Glycated haemoglobin (HbA1c) IVD, calibrator FDA UDI
Device Name
VARIANT II Hemoglobin A1c Program Calibrator/Diluent Set FDA UDI
Model / Reference
270-2115NU FDA UDI
Description
VARIANT II Hemoglobin A1c Program Calibrator/Diluent Set FDA UDI

Identifiers

Catalog Number
2702115NU FDA UDI
Primary DI / UDI-DI
00847817011979 FDA UDI
510(k) Number
K070452 FDA UDI
FDA Product Code
KRZ FDA UDI
LCP FDA UDI
GMDN Term
Glycated haemoglobin (HbA1c) IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.8165 FDA UDI
864.7470 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, calibrator

VARIANT II Hemoglobin A1c 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, calibrator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fb4061b5-af12-4330-aaa8-c9073604e0e2 37 fields · synced May 30, 2026