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Cochlear® Standard Rechargeable Battery Module (Brown, SR2)

by Cochlear Limited

Ref P1711693

Active European Union

CE MDR

Valid until

24 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 Number9321502CP1001_2RechBat4N Basic UDI-DI 09321502054454UDI-DIDate22 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 078611 0132 Active Reissued

    Technical documentation EU MDR

    Issued
    1 Jun 2026
    Expires
    24 Jun 2031
    Valid from
    25 Jun 2026

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Cochlear™ Standard Rechargeable Battery Module
Model / Reference
P1711693
Primary DI / UDI-DI
09321502054454
Basic UDI-DI
9321502CP1001_2RechBat4N
EMDN Code
J0380 Auditory active-implantable devices - accessories
Device Class
Class III
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

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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