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myCochlear™ Connect App (v 8.0, Android, CA-2)

by Cochlear Limited

Ref P2450355

Active European Union

CE MDR

Valid until

21 Jun 2031

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 NumberG70 078611 0116 Date30 Jul 2026IssuedStatusActive expires 21 Jun 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 078611 0116 Active Supplemented

    Technical documentation EU MDR

    Issued
    30 Jul 2026
    Expires
    21 Jun 2031
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
myCochlear™ Connect App
Model / Reference
P2450355
Primary DI / UDI-DI
09321502086486
Basic UDI-DI
9321502myCochlearAppYP
EMDN Code
J0380 Auditory active-implantable devices - accessories
Device Class
Class III
Special Device Type
Software
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