FDA Adverse Event
No answer provided
Summary report: N
COR18001925-000
MDR report key: 8191743
·
Received December 21, 2018
Report
- Report Number
- COR18001925-000
- Event Type
- No answer provided
- Date Received
- December 21, 2018
- Report Date
- December 19, 2018
- Product Code
- GEX
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1027673 | GEX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |