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Tensel Double Smart Me 2015

by MINEL Elektronikai és Kereskedelmi Kft.

Ref TENSEL DOUBLE SMART ME 2015

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 linked in EUDAMED

A group certificate may exist

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 Number5999883347PKGVN Basic UDI-DI 59998833470274UDI-DIDate4 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Tensel
Model / Reference
TENSEL DOUBLE SMART ME 2015
Primary DI / UDI-DI
59998833470274
Basic UDI-DI
5999883347PKGVN
EMDN Code
N010299, U070299, Z120604, Z120621, Z120622, Z12062701, Z12062801, Z12101106
Device Class
Class IIa
Medical Purpose
Nerve and muscle stimulation, TENS/EMS treatment, optional iontophoresis.

Manufacturer details

EUDAMED SRN
HU-PR-000040863

Other devices from MINEL Elektronikai és Kereskedelmi Kft.

Properties

Other properties (1)

  • Sterile: No