← Back to catalogue

β2-MG Fast Test Kit (Immunofluorescence Assay)

EUDAMED

Class B (EU MDR)

Ref IF5011

by Getein Biotech, Inc.

Identity

Trade Name
β2-MG Fast Test Kit (Immunofluorescence Assay) EUDAMED
Device Name
β2-MG Fast Test Kit (Immunofluorescence Assay) EUDAMED
Model / Reference
IF5011 EUDAMED

Identifiers

Primary DI / UDI-DI
06954414792683 EUDAMED
Basic UDI-DI
695441470211GT EUDAMED
EMDN Code
W0102039002 BETA2-MICROGLOBULIN EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

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

Category: Beta-2-microglobulin IVD, reagent

β2-MG Fast Test Kit (Immunofluorescence Assay) by Getein Biotech, Inc. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Beta-2-microglobulin IVD, reagent.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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

Manufacturer

EUDAMED SRN
CN-MF-000017986
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED cbd7bb23-9b1b-4f2f-a5a6-a81a421430fd 61 fields · synced Aug 2, 2026