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FinnComfort

by Waldi Schuhfabrik GmbH 1,000+ variants

Ref 05003-903112

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 Number4030457-FinnCo-001-MN Basic UDI-DI Date8 May 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  • Withdrawn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

Model / Reference
05003-903112
Primary DI / UDI-DI
04030457508510, 04030457508541, 04030457508534, 04030457508503, 04030457508527, 04030457508497, 04030457508466, 04030457508558
Basic UDI-DI
4030457-FinnCo-001-MN
Direct Marketing DI
04030457508510
04030457508541
04030457508534
04030457508503
04030457508527
04030457508497
04030457508466
04030457508558
EMDN Code
Y063303 Ready-made orthotic shoes
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000016907

Other devices from Waldi Schuhfabrik GmbH

See all devices from Waldi Schuhfabrik GmbH →

Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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