FDA Adverse Event
Other
Summary report: N
8044101-2001-00001
MDR report key: 336338
·
Received June 5, 2001
Report
- Report Number
- 8044101-2001-00001
- Event Type
- Other
- Date Received
- June 5, 2001
- Date of Event
- May 9, 2001
- Product Code
- MBU
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 25779 | MBU |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |