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Cochlear™ P1550927

by Cochlear

Part of a family of 56 devices: see the family page

Ref P1550927

Cochlear™ P1550927 is a Class III device made by Cochlear, registered in EUDAMED on 6 Jul 2026 (Basic UDI-DI 9321502CP1000CoilKW) with CE/MDR certificate G70 078611 0133 valid until 12 Jul 2031, approved under FDA PMA P970051 on 25 Jun 1998 and listed in FDA GUDID since 8 Jul 2020 (UDI-DI 09321502049252), active as of 23 Oct 2026. 3 FDA recalls are linked to it.

Active European Union and United States. Also listed in GUDID (US).

CE MDR PMA

Valid until

12 Jul 2031

CE MDR certificate

FDA recalls

None ongoing

3 closed

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

PMA P970051

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number9321502CP1000CoilKW Basic UDI-DI 09321502049252UDI-DIDate6 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number09321502049252 UDI-DI Date8 Jul 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA PMAAPPR GUDID from GUDID Approved NumberP970051 Date25 Jun 1998DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 9321502CP1000CoilKW registered 6 Jul 2026 Active· +1 more in the status table
  • FDA PMA P970051 decided 25 Jun 1998 Active
  • FDA GUDID UDI-DI 09321502049252 listed 8 Jul 2020 Listed

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 078611 0133 Active Reissued

    Technical documentation EU MDR

    Issued
    29 Jun 2026
    Expires
    12 Jul 2031
    Valid from
    13 Jul 2026

Recalls

3 recalls · FDA

    • Terminated Z-2155-2015 FDA Class II initiated 5 Jun 2015

    Cochlear Americas is recalling Nucleus Sterile Silicone Template CI24RE/CI422 part number Z421736 because expired product was distributed.

    • Terminated Z-0003-2012 FDA Unclassified (pre-2012) initiated 16 Sep 2011

    Cochlear implant may shut down and cease to function.

    • Terminated Z-0119-2010 FDA Unclassified (pre-2012) initiated 30 Sep 2009

    Cochlear implant device component was mis-labeled.

Timeline

8 dated events

  1. Approved FDA PMA P970051
  2. Recall initiated FDA recalls Z-0119-2010
  3. Recall initiated FDA recalls Z-0003-2012
  4. Recall initiated FDA recalls Z-2155-2015
  5. Listed FDA GUDID 09321502049252
  6. Certificate issued EUDAMED G70 078611 0133
  7. Registered EUDAMED 9321502CP1000CoilKW
  8. Certificate expires EUDAMED G70 078611 0133

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA PMA Active

Specification

EUDAMED · GUDID

Trade name
Cochlear® Slimline™ Coil (N22) (Black, 11 cm (4")) EUDAMED
Cochlear™ GUDID
Generic name
Cochlear implant/auditory brainstem implant external coil
Device name
Cochlear® Slimline™ Coil
Model / Ref / Catalog
P1550927
Primary DI / UDI-DI
09321502049252
Basic UDI-DI
9321502CP1000CoilKW
PMA number
FDA product code
MCM
EMDN code
J0380 Auditory active-implantable devices - accessories
GMDN term
Cochlear implant/auditory brainstem implant external coil
Device class
Class III
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

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Other devices filed under AUDITORY ACTIVE-IMPLANTABLE DEVICES - ACCESSORIES.

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Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)