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Gymna-Uniphy

by ZMI Electronics Ltd. 22 variants

Ref LP812-340481

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471987233LPYV Basic UDI-DI 04719872331520UDI-DIDate8 Jan 2022RegisteredStatusActive

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  • Withdrawn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
Rubber Electrode
Model / Reference
LP812-340481
Primary DI / UDI-DI
04719872331520
Basic UDI-DI
471987233LPYV
EMDN Code
Z120601 Electrotherapy equipment (included tens)
Device Class
Class I
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
TW-MF-000003571
Authorised representative
mdi Europa GmbH DE-AR-000006218

Other devices from Zmi Elecronics, Ltd.

See all devices from Zmi Elecronics, Ltd. →

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