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Cochlear® Nucleus® Aqua Accessory (5 pcs)

by Cochlear Limited

Ref Z410306

Active European Union

CE MDR

Valid until

5 Apr 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

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 Number9321502AquaAccSURT Basic UDI-DI 09321502022774UDI-DIDate9 Oct 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 078611 0158 Active Supplemented

    Technical documentation EU MDR

    Issued
    11 Sep 2025
    Expires
    5 Apr 2028
    Reason
    Add device or group

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Nucleus® Aqua Accessory
Model / Reference
Z410306
Primary DI / UDI-DI
09321502022774
Basic UDI-DI
9321502AquaAccSURT
Unit of Use DI
09321502060387
EMDN Code
J0380 Auditory active-implantable devices - accessories
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
AU-MF-000009890
Authorised representative
Cochlear Deutschland GmbH & Co. KG DE-AR-000006034

Other devices from Cochlear Ltd

See all devices from Cochlear Ltd →

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