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Immunoglobulin G Reagent (Ig-G 2 x 150)

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 467925

by Beckman Coulter Inc.

Identity

Trade Name
Immunoglobulin G Reagent (Ig-G 2 x 150) EUDAMED
Synchron FDA UDI
Generic Name
Total immunoglobulin G (IgG total) IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Immunoglobulin G Reagent (Ig-G 2 x 150) EUDAMEDFDA UDI
Model / Reference
467925 EUDAMEDFDA UDI
Description
Immunoglobulin G Reagent (Ig-G 2 x 150) FDA UDI

Identifiers

Catalog Number
467925 FDA UDI
Primary DI / UDI-DI
D-467925RT EUDAMED
15099590231613 FDA UDI
Basic UDI-DI
B-467925RT EUDAMED
FDA Product Code
DEW FDA UDI
EMDN Code
W0102010105 IMMUNOGLOBULIN G EUDAMED
GMDN Term
Total immunoglobulin G (IgG total) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
866.5510 FDA UDI
Market of Registration
Ireland 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

No

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

Prescription Use

Yes

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: Human immunoglobulin G (IgG) animal conjugate antibody reagent IVD

Immunoglobulin G Reagent (Ig-G 2 x 150) by Beckman Coulter, Inc. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Human immunoglobulin G (IgG) animal conjugate antibody reagent IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000010288
Authorised Representative
Beckman Coulter Ireland Inc. IE-AR-000000886

Sources (2)

  • EUDAMED c4f45ab8-a363-4d10-93d7-57d78db8d395 61 fields · synced Oct 7, 2026
  • FDA UDI 412b5bf2-4f65-4a01-bc24-3ea9f7b90e5a 34 fields · synced May 30, 2026