FDA Adverse Event
Injury
Summary report: N
BIA400 IMPLANT 4MM W ABUTMENT 10MM
MDR report key: 8770160
·
Received July 8, 2019
Report
- Report Number
- 6000034-2019-01201
- Event Type
- Injury
- Date Received
- July 8, 2019
- Report Date
- June 20, 2019
- Manufacturer
- COCHLEAR BONE ANCHORED SOLUTIONS AB
- Product Code
- MAH
- UDI-DI
- 09321502022712
- Adverse Event
- Yes
- Report Source
- Distributor report
- Reporter Location
- NY, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THIS REPORT IS FILED ON JULY 09, 2019.
Description of Event or Problem · 1
PER THE CLINIC THE PATIENT EXPERIENCED CHRONIC INFECTIONS AT ABUTMENT SITE, CLINICAL MANAGEMENT IS ONGOING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 560182 | BIA400 IMPLANT 4MM W ABUTMENT 10MM | COCHLEAR BAHA CONNECT SYSTEM | MAH | COCHLEAR BONE ANCHORED SOLUTIONS AB | 93331 | 175760 | 09321502022712 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |