← Back to catalogue

Anti-Leb (Murine Monoclonal) Gamma-clone Blood Grouping Reagent

EUDAMEDFDA UDI

Class C (EU MDR)

Ref 0004864

by Immucor, Inc.

Identity

Trade Name
Anti-Leb (Murine Monoclonal) Gamma-clone Blood Grouping Reagent EUDAMED
Anti-Leb (Murine Monoclonal) Gamma-clone FDA UDI
Generic Name
Anti-Le^b red blood cell grouping IVD, antibody FDA UDI
Device Name
Anti-Leb (Murine Monoclonal) Gamma-clone EUDAMED
This reagent is used for the detection of the Leb antigen (of the Lewis system) on red blood cells by tube test. This product configuration is a single vial. FDA UDI
Model / Reference
0004864 EUDAMEDFDA UDI
Description
This reagent is used for the detection of the Leb antigen (of the Lewis system) on red blood cells by tube test. This product configuration is a single vial. FDA UDI

Identifiers

Catalog Number
0004864 FDA UDI
Primary DI / UDI-DI
10888234001898 EUDAMEDFDA UDI
Basic UDI-DI
88823401W0103030501C101SK EUDAMED
EMDN Code
W0103030501 OTHER ANTIGEN TYPING REAGENTS EUDAMED
GMDN Term
Anti-Le^b red blood cell grouping IVD, antibody FDA UDI

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

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

Anti-Leb (Murine Monoclonal) Gamma-clone Blood Grouping Reagent by Immucor, Inc. — Class C — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Immucor, Inc.
EUDAMED SRN
US-MF-000011568
Authorised Representative
IMMUCOR Medizinische Diagnostik GmbH DE-AR-000007083

Sources (2)

  • EUDAMED 3d99c4bd-4966-4d77-9cc2-93b47396f2d8 61 fields · synced Oct 6, 2026
  • FDA UDI a062ba1f-e923-4d7c-9ca4-57281bd824a5 35 fields · synced May 30, 2026