FDA Adverse Event
Malfunction
Summary report: N
8010042-2008-00095
MDR report key: 1161963
·
Received July 8, 2008
Report
- Report Number
- 8010042-2008-00095
- Event Type
- Malfunction
- Date Received
- July 8, 2008
- Product Code
- CBK
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CBK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |