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Cl Aia-Pack Sample Diluting Reagent F

EUDAMED

Class IVD General (EU MDR)

Ref 0029406

by Tosoh Corporation

Identity

Trade Name
CL AIA-PACK SAMPLE DILUTING REAGENT F EUDAMED
Device Name
CL AIA-PACK SAMPLE DILUTING REAGENT F EUDAMED
Model / Reference
0029406 EUDAMED

Identifiers

Primary DI / UDI-DI
14560189215754 EUDAMED
Basic UDI-DI
B-14560189215754 EUDAMED
45601892100010467G EUDAMED
EMDN Code
W01029003 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC) EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Class A EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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 Sample Diluting Reagent F by Tosoh Corporation — Class IVD General — IVDR, IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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 (2)

  • EUDAMED e35da70b-e8cd-46d5-8e92-83d4d876071e 61 fields · synced Jul 31, 2026
  • EUDAMED 1a494e5b-d19e-4ddd-8b66-bab375ac86a5 61 fields · synced May 17, 2026