Electrodos TENS LESSA

by AB Medica Group S.A 33 variants

Ref 8711901

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number842876387TENSELECTCY Basic UDI-DI 08428763027478UDI-DI	Date6 Oct 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Electrodos para electroestimulación
Model / Reference: 8711901

Primary DI / UDI-DI: 08428763027478
Basic UDI-DI: 842876387TENSELECTCY
EMDN Code: N010201 Tens system electrodes

Device Class: Class I
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: ES-MF-000000582

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Electrodos TENS LESSA

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Electrodos reutilizables para electrocardiografía LESSA

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Adaptadores de conexión para electrodos desechables y reutilizables LESSA

Class I
Papeles de Registro médico LESSA

Class I

See all devices from Ab Medica Group S. a. →

Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No