FDA Adverse Event
Injury
Summary report: N
BA400 ABUTMENT 10MM
MDR report key: 9838334
·
Received March 16, 2020
Report
- Report Number
- 6000034-2020-00710
- Event Type
- Injury
- Date Received
- March 16, 2020
- Report Date
- February 19, 2020
- Manufacturer
- COCHLEAR BONE ANCHORED SOLUTIONS AB
- Product Code
- MAH
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
THIS REPORT IS SUBMITTED ON MARCH 16, 2020.
Description of Event or Problem · 1
PER THE CLINIC, THE PATIENT HAD AN ABUTMENT REPLACEMENT (REASON UNKNOWN) UNDER A GENERAL ANAESTHETIC (DATE UNKNOWN).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 298139 | BA400 ABUTMENT 10MM | COCHLEAR BAHA CONNECT SYSTEM | MAH | COCHLEAR BONE ANCHORED SOLUTIONS AB | 93335 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |