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CL AIA-PACK β2-Microglobulin TEST CUP

EUDAMED

Class IVD General (EU MDR)

Ref 0029141

by Tosoh Corporation

Identity

Device Name
CL AIA-PACK β2-Microglobulin TEST CUP EUDAMED
Model / Reference
0029141 EUDAMED

Identifiers

Primary DI / UDI-DI
14562185400936 EUDAMED
Basic UDI-DI
B-14562185400936 EUDAMED
EMDN Code
W0102039002 BETA2-MICROGLOBULIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

Category: Beta-2-microglobulin IVD, reagent

CL AIA-PACK β2-Microglobulin TEST CUP by Tosoh Corporation — Class IVD General — IVDD — 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/IVDD

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Manufacturer

Manufacturer
Tosoh Corporation
EUDAMED SRN
JP-MF-000024143
Authorised Representative
Tosoh Europe N.V. BE-AR-000000211

Sources (1)

  • EUDAMED cac2edcd-62d9-4488-8d79-035f8aa8b3e8 61 fields · synced Jun 19, 2026