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Elasticated Ankle Support Extra Large

by Fima Global Brands Ltd 2 variants

Ref FT-1102-XL(1)BEIGEModel FORTUNA -ELASTICATED ANKLE SUPPORT

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506098242FT-1102-S-XXL2M Basic UDI-DI 05060982423117UDI-DIDate28 Nov 2025RegisteredStatusActive

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  • Withdrawn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
Fortuna -Elasticated Ankle Support
Model / Reference
FORTUNA -ELASTICATED ANKLE SUPPORT, FT-1102-XL(1)BEIGE
Primary DI / UDI-DI
05060982423117
Basic UDI-DI
506098242FT-1102-S-XXL2M
EMDN Code
Y06120601 Passive ankle-foot orthoses
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
UK-MF-000036604
Authorised representative
GLORY-Cosmetic Hungary Kft. HU-AR-000035374

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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