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Dormo

by Telic, S.A.U. 21 variants

Part of a family of 8 devices: see the family page

Ref LF-50T

Dormo (LF-50T) is a Class I device made by Telic, S.A.U., registered in EUDAMED on 20 Aug 2024 (Basic UDI-DI 8427734ECGELECVL), active as of 7 Nov 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8427734ECGELECVL Basic UDI-DI 08427734036884UDI-DIDate20 Aug 2024RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
ECG electrodes Ag/AgCl
Model / reference
LF-50T
Primary DI / UDI-DI
08427734036884
Basic UDI-DI
8427734ECGELECVL
EMDN code
C020501 ECG electrodes
Device class
Class I
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000001853

Related devices

Category: Electrocardiographic electrode, single-use

Similar devices in this category

Other devices filed under ECG ELECTRODES.

Other devices from Telic, S.A.U.

See all devices from Telic, S.A.U. →

Properties

Other properties (14, all answered No)