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Electroencephalograph EEG-1200K

EUDAMED

Class IIa (EU MDR)

Ref EEG-1200K-NE

by Nihon Kohden Corporation

Identity

Trade Name
Electroencephalograph EEG-1200K EUDAMED
Device Name
Electroencephalograph EUDAMED
Model / Reference
EEG-1200K-NE EUDAMED

Identifiers

Primary DI / UDI-DI
04931921050170 EUDAMED
Basic UDI-DI
4931921MD2a0014LQ EUDAMED
EMDN Code
Z12100302 ELECTROENCEPHALOGRAPHS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Electroencephalograph EEG-1200K by Nihon Kohden Corporation — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
JP-MF-000019022
Authorised Representative
NIHON KOHDEN EUROPE GmbH DE-AR-000010740

Sources (1)

  • EUDAMED 48d3b3a2-1b88-496b-aea7-c1dc192773b0 61 fields · synced Jul 29, 2026