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Cl Aia-Pack Diluent Concentrate

EUDAMED

Class A (EU MDR)

Ref 0029708

by Tosoh Corporation

Identity

Trade Name
CL AIA-PACK DILUENT CONCENTRATE EUDAMED
Device Name
CL AIA-PACK DILUENT CONCENTRATE EUDAMED
Model / Reference
0029708 EUDAMED

Identifiers

Primary DI / UDI-DI
04560189213630 EUDAMED
Basic UDI-DI
456018921000100572 EUDAMED
EMDN Code
W01029099 IMMUNOCHEMISTRY REAGENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Cl Aia-Pack Diluent Concentrate by Tosoh Corporation — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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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 1fa792a1-57c2-4c57-a117-890f61eb520b 61 fields · synced Jun 19, 2026