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Alpha2-macroglobulin

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 9029524190

by Diagam S.A.

Identity

Trade Name
Alpha2-macroglobulin EUDAMEDFDA UDI
Generic Name
Alpha-2-macroglobulin IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Alpha2-macroglobulin EUDAMED
In vitro diagnostic reagent for the quantitative determination of alpha2macroglobulin in samples of human origin (serum, heparinized plasma) by immunoturbidimetry on the cobas c systems. FDA UDI
Model / Reference
9029524190 EUDAMED
09029524190 FDA UDI
Description
In vitro diagnostic reagent for the quantitative determination of alpha2macroglobulin in samples of human origin (serum, heparinized plasma) by immunoturbidimetry on the cobas c systems. FDA UDI

Identifiers

Catalog Number
09029524190 FDA UDI
Primary DI / UDI-DI
05415168006873 EUDAMEDFDA UDI
Basic UDI-DI
B-05415168006873 EUDAMED
FDA Product Code
DEB FDA UDI
EMDN Code
W0102019003 A2-MACROGLOBULIN EUDAMED
GMDN Term
Alpha-2-macroglobulin IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
866.5620 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Alpha2-macroglobulin by Diagam S.A. — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diagam S.A.
EUDAMED SRN
BE-MF-000022993

Sources (2)

  • EUDAMED 1b6b6c7f-3ed7-48b3-b457-a2c1c33f4b8e 61 fields · synced Jun 19, 2026
  • FDA UDI 349a46f4-4ac9-46e0-84c8-1dba8ceaf106 35 fields · synced May 30, 2026