RONDO Control Unit ebony 08477
by Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number09008737084776 | Date22 Sep 2014 | StatusListed |
Recalls
-
- Ongoing Z-2356-2024
A small number of devices may have a higher probability of a crack within the internal electronics substrate which could result in a non-functional device.
-
- Terminated Z-2138-2019
- Terminated Z-2136-2019
- Terminated Z-2137-2019
Devices were distributed despite the Helium-fine leak test results not being within the cochlear implant standards specification.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- RONDO Control Unit ebony
- Generic Name
- Cochlear implant/auditory brainstem implant sound processor
- Model / Reference
- 08477
- Primary DI / UDI-DI
- 09008737084776
- PMA Number
- FDA Product Code
- MCM
- GMDN Term
- Cochlear implant/auditory brainstem implant sound processor
- Device Class
- Class III
- GUDID distribution status
- Not in Commercial Distribution
- MRI Safety
- MR Unsafe
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Properties
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No