FDA Adverse Event
Malfunction
Summary report: N
8031673-2005-00024
MDR report key: 643743
·
Received September 13, 2005
Report
- Report Number
- 8031673-2005-00024
- Event Type
- Malfunction
- Date Received
- September 13, 2005
- Date of Event
- August 25, 2005
- 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 |