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HCGSN 230 MR LTM: 32 ch Pediatric Small 47-51 cm AGeodesic EEG System (GES) 2 AND UP ONLY

by Magstim Inc.

Ref 4750051

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-4750051YT Basic UDI-DI D-4750051YTUDI-DIDate8 Jul 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
HCGSN 230 MR LTM: 32 ch Pediatric Small 47-51 cm AGeodesic EEG System (GES) 2 AND UP ONLY
Model / Reference
4750051
Primary DI / UDI-DI
D-4750051YT
Basic UDI-DI
B-4750051YT
EMDN Code
Z12100303 Systems for analysing and managing EEG traces
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000024844
Authorised representative
MPS Medical Product Service GmbH DE-AR-000005009

Other devices from Magstim Inc.

See all devices from Magstim Inc. →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No