FDA Adverse Event
No answer provided
Summary report: N
COR24000010-000
MDR report key: 18487641
·
Received January 10, 2024
Report
- Report Number
- COR24000010-000
- Event Type
- No answer provided
- Date Received
- January 10, 2024
- Report Date
- December 20, 2023
- Product Code
- GEX
- Report Source
- Manufacturer report
- Reporter Location
- IT
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 606223 | GEX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |