FDA Adverse Event
Death
Summary report: N
1043565-2003-00001
MDR report key: 460107
·
Received May 13, 2003
Report
- Report Number
- 1043565-2003-00001
- Event Type
- Death
- Date Received
- May 13, 2003
- Date of Event
- February 7, 2003
- 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 |