A device designed to be used with a cochlear implant (CI) or auditory brainstem implant system to connect the sound processor to power options (e.g., battery pack) and/or to enable connections to external devices that may be used as peripherals to the implant
| Company | Devices | Share |
|---|---|---|
| Cochlear Limited | 88 | 97% |
| Med-El Elektromedizinische Geräte Gesellschaft M.B.H. | 3 | 3% |
Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| MCM | IMPLANT, COCHLEAR | 82 |
| MCM | Implant, cochlear | 4 |
| MCM | Implant, Cochlear | 3 |
| PFO | Active implantable bone conduction hearing system | 2 |
| PGQ | Hybrid cochlear implant | 1 |
Use these as the dimensions to specify in a tender line.
91 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cochlear implant/auditory brainstem implant peripheral connector", from 2 companies. The largest labeler is Cochlear Limited with 97% of records.
MCM (IMPLANT, COCHLEAR), MCM (Implant, cochlear), MCM (Implant, Cochlear), PFO (Active implantable bone conduction hearing system)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.