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Parma

by Florett GmbH

Ref 60922Model Genua; Malmö; Stockholm; Göteborg; Lugano; Genf; Dublin; Rijeka; Meran; Hamburg; Kokolla; Tromsö; Zürich; Vancouver; Rhodos; Dover; Rimini; Florenz; Parma; London; Belfast; Garmisch; Lindau; München; Innsbruck; Villach

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4040261therapieUE Basic UDI-DIDate12 Oct 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  • Withdrawn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

Device Name
Therapieschuhe
Model / Reference
Genua, Malmö, Stockholm, Göteborg, Lugano, Genf, Dublin, Rijeka, Meran, Hamburg, Kokolla, Tromsö, Zürich, Vancouver, Rhodos, Dover, Rimini, Florenz, Parma, London, Belfast, Garmisch, Lindau, München, Innsbruck, Villach, 60922
Primary DI / UDI-DI
04040261118041, 04040261118072, 04040261118089, 04040261117990, 04040261118065, 04040261117983, 04040261118027, 04040261118058, 04040261118003, 04040261117976, 04040261118034, 04040261118010
Basic UDI-DI
4040261therapieUE
EMDN Code
Y063303 Ready-made orthotic shoes
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000012054

Other devices from Florett GmbH

See all devices from Florett GmbH →

Properties

  • Animal Tissues

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No