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RF Cable

by Advanced Bionics LLC 15 variants

Ref CI-5415-606

Active European Union

CE MDR

Valid until

6 Feb 2029

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 077725 0027 Date2 Sep 2026IssuedStatusActive expires 6 Feb 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 077725 0027 Active Supplemented

    Technical documentation EU MDR

    Certifier
    TÜV SÜD Product Service GmbH 0123
    Issued
    2 Sep 2026
    Expires
    6 Feb 2029
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
CI-5415-606
Primary DI / UDI-DI
00840094471375
Basic UDI-DI
08400944CI5415Y4
EMDN Code
J0380 Auditory active-implantable devices - accessories
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000019344
Authorised representative
Advanced Bionics GmbH DE-AR-000005642

Other devices from Advanced Bionics

See all devices from Advanced Bionics →

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