FDA Adverse Event
Injury
Summary report: N
2025501-1997-00881
MDR report key: 116895
·
Received August 29, 1997
Report
- Report Number
- 2025501-1997-00881
- Event Type
- Injury
- Date Received
- August 29, 1997
- Product Code
- DZE
- Adverse Event
- Yes
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | Implant | DZE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |