Skip to content

Foot Pain Electrode

by TensCare Ltd

Part of a family of 7 devices: see the family page

Ref E-ALFTModel Aliment Electrode

Foot Pain Electrode (E-ALFT) is a medical device (EU MDR Class I; EMDN category tens system electrodes) made by TensCare Ltd, registered in EUDAMED on 20 Feb 2025 (Basic UDI-DI 5033435E00070X5), 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 Number5033435E00070X5 Basic UDI-DI 05033435144211UDI-DIDate20 Feb 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device name
Aliment Electrode
Model / reference
Aliment Electrode, E-ALFT
Primary DI / UDI-DI
05033435144211
Basic UDI-DI
5033435E00070X5
EMDN code
N010201 Tens system electrodes
Device class
Class I
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
GB-MF-000004156
Authorised representative
Advena Limited MT-AR-000000234

Similar devices in this category

Other devices filed under TENS SYSTEM ELECTRODES.

Other devices from TensCare Ltd

See all devices from TensCare Ltd →

Properties

Other properties (14, all answered No)