FDA Adverse Event
No answer provided
Summary report: N
COR20000306-000
MDR report key: 10969177
·
Received December 8, 2020
Report
- Report Number
- COR20000306-000
- Event Type
- No answer provided
- Date Received
- December 8, 2020
- Report Date
- November 11, 2020
- Product Code
- KPR
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1428879 | KPR |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |