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Electrode K

EUDAMED

Class B (EU MDR)

Ref 0018263500

by Instrumentation Laboratory SpA

Identity

Trade Name
Electrode K EUDAMED
Device Name
Electrode K EUDAMED
Model / Reference
0018263500 EUDAMED

Identifiers

Primary DI / UDI-DI
08426950038160 EUDAMED
Basic UDI-DI
84269500381606A EUDAMED
Direct Marketing DI
08426950038160 EUDAMED
EMDN Code
W0101070106 POTASSIUM - ELECTRODES EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Italy 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

Electrode K by Instrumentation Laboratory SpA — 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
IT-MF-000009277

Sources (1)

  • EUDAMED f3decc18-b64f-4509-8d72-07d0d40a47ea 61 fields · synced Jul 9, 2026