FDA Adverse Event
Injury
Summary report: N
9610200-2007-00009
MDR report key: 1033478
·
Received November 14, 2007
Report
- Report Number
- 9610200-2007-00009
- Event Type
- Injury
- Date Received
- November 14, 2007
- Product Code
- MOZ
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MOZ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |