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Desfi-Dormo

by Telic, S.A.U. 41 variants

Ref EDC-P220

Desfi-Dormo (EDC-P220) is a Class I device made by Telic, S.A.U., registered in EUDAMED on 14 May 2025 (Basic UDI-DI B-08427734008553), active as of 24 Oct 2026.

Active European Union

CE MDD

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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08427734008553 Basic UDI-DI 08427734008553UDI-DIDate14 May 2025RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device name
Electrodos de desfibrilación con cable pediátricos
Model / reference
EDC-P220
Primary DI / UDI-DI
08427734008553
Basic UDI-DI
B-08427734008553
EMDN code
C020480 Cardioversion and external defibrillation devices - accessories
Device class
Class I
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000001853

Similar devices in this category

Other devices filed under EXTERNAL CARDIOVERSION AND DEFIBRILLATION DEVICES.

Other devices from Telic, S.A.U.

See all devices from Telic, S.A.U. →

Properties

Other properties (12, all answered No)