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EGI Response Pad/Chronos Adapter Bundle

EUDAMED

Class IIa (EU MDR)

Ref 4609754

by Magstim Inc.

Identity

Device Name
EGI Response Pad/Chronos Adapter Bundle EUDAMED
Model / Reference
4609754 EUDAMED

Identifiers

Primary DI / UDI-DI
D-460975422 EUDAMED
Basic UDI-DI
B-460975422 EUDAMED
EMDN Code
Z12100303 SYSTEMS FOR ANALYSING AND MANAGING EEG TRACES 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

EGI Response Pad/Chronos Adapter Bundle by Magstim Inc. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Magstim Inc.
EUDAMED SRN
US-MF-000024844
Authorised Representative
MPS Medical Product Service GmbH DE-AR-000005009

Sources (1)

  • EUDAMED e29a8faf-7d3b-4041-92c0-7be2334b059d 61 fields · synced Jun 19, 2026