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GLORY Szilikonos sarokemelő (Férfi) M 1 Darab

by GLORY-Cosmetic Hungary Korlátolt Felelősségű Társaság

Ref SH002Model GLORY Lábápolási eszközök

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

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5999863752GSZTVY Basic UDI-DI Date25 Jun 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  • Withdrawn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

Trade Name
GLORY Szilikonos sarokemelő (Férfi) M 1 Darab
GLORY Szilikonos sarokemelő (Férfi) S 1 Darab
GLORY Szilikonos sarokemelő (Férfi) L 1 Darab
Device Name
GLORY Lábápolási eszközök
Model / Reference
GLORY Lábápolási eszközök, SH002
Primary DI / UDI-DI
05999887733666, 05999887733475, 05999887733673
Basic UDI-DI
5999863752GSZTVY
EMDN Code
Y061203 Orthoses, foot (including insoles and inserts)
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
HU-MF-000053501

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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