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FinnComfort

by Waldi Schuhfabrik GmbH 1,000+ variants

Ref 02557-503218

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  • Withdrawn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
02557-503218
Primary DI / UDI-DI
04030457005552, 04030457005583, 04030457005651, 04030457005644, 04030457005613, 04030457005590, 04030457005637, 04030457005606, 04030457005576, 04030457005620, 04030457005668, 04030457005569
Basic UDI-DI
4030457-FinnCo-001-MN
Direct Marketing DI
04030457005552
04030457005583
04030457005651
04030457005644
04030457005613
04030457005590
04030457005637
04030457005606
04030457005576
04030457005620
04030457005668
04030457005569
EMDN Code
Y063303 Ready-made orthotic shoes
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000016907

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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