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Ortopedická obuv pre diabetikov

by diawin Deutschland GmbH 49 variants

Ref AF16412Model midnight tulip 41 wide

Active European Union

CE MDD

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/MDD NumberB-04260502823095 Basic UDI-DI 04260502823095UDI-DIDate10 Jul 2024RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Ortopedická obuv pre diabetikov
Model / Reference
midnight tulip 41 wide, AF16412
Primary DI / UDI-DI
04260502823095
Basic UDI-DI
B-04260502823095
EMDN Code
Y063303 Ready-made orthotic shoes
Device Class
Class I
EU market of registration
Slovakia

Manufacturer details

EUDAMED SRN
DE-MF-000040108

Other devices from diawin Deutschland GmbH

See all devices from diawin Deutschland GmbH →

Properties

Other properties (11)

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