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Anti-A, B (Murine Monoclonal Blend) Series 1

FDA UDI

by Immucor, Inc.

Identity

Trade Name
Anti-A,B (Murine Monoclonal Blend) Series 1 FDA UDI
Generic Name
Anti-AB red blood cell grouping IVD, antibody FDA UDI
Device Name
This product is intended for use in slide, tube, and microplate tests, for the detection of both the A and B antigens. FDA UDI
Model / Reference
0006408 FDA UDI
Description
This product is intended for use in slide, tube, and microplate tests, for the detection of both the A and B antigens. FDA UDI

Identifiers

Catalog Number
0006408 FDA UDI
Primary DI / UDI-DI
10888234000549 FDA UDI
GMDN Term
Anti-AB red blood cell grouping IVD, antibody FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

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

No

FDA UDI

Category: Anti-AB red blood cell grouping IVD, antibody

Anti-A, B (Murine Monoclonal Blend) Series 1 by Immucor, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anti-AB red blood cell grouping IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Immucor, Inc.

Sources (1)

  • FDA UDI 1b1e1d4c-376f-4e2d-b8f9-0d9c55351d95 35 fields · synced Jun 6, 2026