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Reference Electrode Kit

EUDAMED

Class B (EU MDR)

Ref 980845

by Thermo Fisher Scientific Oy

Identity

Trade Name
Reference Electrode Kit EUDAMED
Device Name
Reference Electrode Kit EUDAMED
Model / Reference
980845 EUDAMED

Identifiers

Primary DI / UDI-DI
16438153808456 EUDAMED
Basic UDI-DI
6438153BU00145BU EUDAMED
Direct Marketing DI
16438153808456 EUDAMED
EMDN Code
W0101070301 REFERENCE ELECTRODES EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Finland 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

Reference Electrode Kit by Thermo Fisher Scientific Oy — Class B — 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

EUDAMED SRN
FI-MF-000001479

Sources (1)

  • EUDAMED 87b69799-3144-4c44-8512-bf038cd1b3a4 61 fields · synced Oct 7, 2026