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BrainAvatar

by BrainMaster Technologies, Inc.

Ref 533-145AModel Discovery 20

BrainAvatar (533-145A) is a Class IIa device made by BrainMaster Technologies, Inc., registered in EUDAMED on 27 Jul 2026 (Basic UDI-DI 0852391007EEG2X), active as of 23 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0852391007EEG2X Basic UDI-DI 00852391007157UDI-DIDate27 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Discovery 20
Model / reference
Discovery 20, 533-145A
Primary DI / UDI-DI
00852391007157
Basic UDI-DI
0852391007EEG2X
Direct marketing DI
00852391007157
EMDN code
Z12100302 Electroencephalographs
Device class
Class IIa
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000008908
Authorised representative
mdi Europa GmbH DE-AR-000006218

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Properties

  • Measuring function
Other properties (13, all answered No)