FDA Adverse Event
Injury
Summary report: N
2183870-2007-00060
MDR report key: 1351433
·
Received February 25, 2009
Report
- Report Number
- 2183870-2007-00060
- Event Type
- Injury
- Date Received
- February 25, 2009
- Product Code
- LIT
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
A MEDWATCH FORM WAS SENT TO EV3 INC BY THE HOSP. THE PT INFO WAS OBTAINED FROM THEIR REPORT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LIT |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |