FDA Adverse Event
Other
Summary report: N
1220413-2001-00001
MDR report key: 372038
·
Received January 11, 2002
Report
- Report Number
- 1220413-2001-00001
- Event Type
- Other
- Date Received
- January 11, 2002
- Date of Event
- December 9, 2001
- 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 |