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E-Eegx

EUDAMED

Class IIb (EU MDR)

Ref E-EEGXModel MJD101

by GE Healthcare Finland Oy

Identity

Device Name
E-EEGX EUDAMED
E-EEGX, N-EEGX EUDAMED
Model / Reference
MJD101 EUDAMED
E-EEGX EUDAMED

Identifiers

Primary DI / UDI-DI
00840682125628 EUDAMED
Basic UDI-DI
B-00840682125628 EUDAMED
8406821BUG00433HF EUDAMED
Direct Marketing DI
00840682125628 EUDAMED
EMDN Code
Z1203020280 MULTI-PARAMETER MONITORS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Finland 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

E-Eegx by GE Healthcare Finland Oy — Class IIb — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
FI-MF-000001176

Sources (2)

  • EUDAMED ec395005-e4db-40f0-8362-029cfbeee52f 61 fields · synced Oct 8, 2026
  • EUDAMED 3dea75b5-5bfb-4923-bb2f-851c8de55006 61 fields · synced May 18, 2026