FDA Adverse Event
No answer provided
Summary report: N
COR16000480-000
MDR report key: 9354097
·
Received September 13, 2016
Report
- Report Number
- COR16000480-000
- Event Type
- No answer provided
- Date Received
- September 13, 2016
- Report Date
- September 13, 2016
- Product Code
- GEX
- Report Source
- Manufacturer report
- Reporter Location
- UT, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 596859 | GEX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |