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Electrode Gel Adapter

EUDAMED

Class I (EU MDR)

Ref 00500

by Bottneuro AG

Identity

Trade Name
Electrode Gel Adapter EUDAMED
Device Name
Miamind Neurostimulator Electrodes EUDAMED
Model / Reference
00500 EUDAMED

Identifiers

Primary DI / UDI-DI
07649988035524 EUDAMED
Basic UDI-DI
76499880355ELECTNF EUDAMED
EMDN Code
N01010202 EEG EXTRACRANIC ELECTRODES EUDAMED

Classification

Device Class
Class I 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Electrode Gel Adapter by Bottneuro AG — Class I — 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

Manufacturer
Bottneuro AG
EUDAMED SRN
CH-MF-000041419
Authorised Representative
Blue Broccoli GmbH LI-AR-000000233

Sources (1)

  • EUDAMED 9b7175d0-266a-460f-8a4b-94d47e5d6ead 61 fields · synced Jun 18, 2026