FDA Adverse Event
Other
Summary report: N
1222081-2008-00005
MDR report key: 1012293
·
Received March 7, 2008
Report
- Report Number
- 1222081-2008-00005
- Event Type
- Other
- Date Received
- March 7, 2008
- Product Code
- ---
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | --- |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |