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FinnComfort

by Waldi Schuhfabrik GmbH 1,000+ variants

Ref 01701-902623

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 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  • Withdrawn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
01701-902623
Primary DI / UDI-DI
00691812802991, 00691812803035, 00691812802984, 00691812803011, 00691812803066, 00691812803028, 00691812803042, 00691812803004, 00691812803059
Basic UDI-DI
4030457-FinnCo-001-MN
Direct Marketing DI
00691812802991
00691812803035
00691812802984
00691812803011
00691812803066
00691812803028
00691812803042
00691812803004
00691812803059
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