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Fortuna

by Fortuna Healthcare Limited 202 variants

Ref FT24EFS1Model FORTUNA FINGER SPLINT

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 Number5031720FT24EFS9R Basic UDI-DIDate24 Sep 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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

Model / Reference
FORTUNA FINGER SPLINT, FT24EFS1
Primary DI / UDI-DI
05031720052647
Basic UDI-DI
5031720FT24EFS9R
EMDN Code
Y060603 Fingers orthoses
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
UK-MF-000048072
Authorised representative
Fortuna Healthcare (Ireland) Limited IE-AR-000044547

Other devices from Fortuna Healthcare Limited

See all devices from Fortuna Healthcare Limited →

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