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Trackit T4A

by Lifelines Ltd.

Ref 2800EUModel Trackit T4A

Trackit T4A (2800EU) is a Class IIa device made by Lifelines Ltd., registered in EUDAMED on 14 Aug 2026 (Basic UDI-DI 506027545T5P9), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506027545T5P9 Basic UDI-DI 05060275450844UDI-DIDate14 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Trackit T4A, 2800EU
Primary DI / UDI-DI
05060275450844
Basic UDI-DI
506027545T5P9
EMDN code
Z12100302 Electroencephalographs
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
GB-MF-000020001
Authorised representative
Incereb Ltd IE-AR-000002462

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Properties

Other properties (14, all answered No)