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Páciens kábel TENSEL DOUBLE SMART ME 2015-höz

by MINEL Elektronikai és Kereskedelmi Korlátolt Felelősségű Társaság

Ref TDSPC-1.5-2

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5999883347CABSD Basic UDI-DI 59998833470892UDI-DIDate5 Aug 2026RegisteredStatusActive

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  • Withdrawn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
Patient Cable
Model / Reference
TDSPC-1.5-2
Primary DI / UDI-DI
59998833470892
Basic UDI-DI
5999883347CABSD
Direct Marketing DI
59998833470892
EMDN Code
Z120601 Electrotherapy equipment (included tens)
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000008069

Other devices from MINEL Elektronikai és Kereskedelmi Korlátolt Felelősségű Társaság

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