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Additionsvernetzendes Ohrabformsilikon

by Innovation MediTech GmbH EUDAMED

Active European Union

Ref 20645

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++E2390057YK Basic UDI-DIDate12 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 44911220478 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0044
    Issued
    17 Nov 2025
    Expires
    4 Dec 2028
    Reason
    Other

Specification

EUDAMED

Device Name
Additionsvernetzendes Ohrabformsilikon
Model / Reference
20645
Primary DI / UDI-DI
+E239206451
Basic UDI-DI
++E2390057YK
EMDN Code
Y214580 Hearing aids or hearing devices - accessories
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005462

Other devices from Innovation Meditech GmbH

See all devices from Innovation Meditech GmbH →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: 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