FDA Adverse Event
Other
Summary report: N
*
MDR report key: 980538
·
Received December 20, 2007
Report
- Report Number
- 1221826-2007-00034
- Event Type
- Other
- Date Received
- December 20, 2007
- Manufacturer
- KARL STORZ ENDOVISION, INC.
- Product Code
- FFZ
- Report Source
- Manufacturer report
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | * | FFZ | KARL STORZ ENDOVISION, INC. | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |