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Fortuna

by Fortuna Healthcare Limited EUDAMED

Active European Union

Ref FT24EP6Model FT24EP/EW/EF/EB/EK

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5031720FT24EHL Basic UDI-DIDate11 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Plasters
Model / Reference
FT24EP/EW/EF/EB/EK, FT24EP6
Primary DI / UDI-DI
05031720052050
Basic UDI-DI
5031720FT24EHL
EMDN Code
M050202 Non-extensible woven plasters
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