Skip to content

Otodynamics

by Otodynamics Ltd United Kingdom EUDAMED

Ref FLX-S +ABR

EMDN Z12140302

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060396171215 Basic UDI-DIDate23 Mar 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Otoport Flexi + Abr
Model / Reference
FLX-S +ABR
Primary DI / UDI-DI
05060396171215
Basic UDI-DI
B-05060396171215
EMDN Code
Z12140302 Evoked potential audiometry equipments
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
GB-MF-000018964
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Otodynamics, Ltd.

See all devices from Otodynamics, Ltd. →

Properties & raw data

Show properties, registry sources and raw records
  • Measuring Function
Other properties (10)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 03f7ad1a-93be-4eda-82ea-b362e40ac464 61 fields · synced 22 Oct 2026