FDA Adverse Event
Other
Summary report: N
COR18001718-000
MDR report key: 8050966
·
Received November 7, 2018
Report
- Report Number
- COR18001718-000
- Event Type
- Other
- Date Received
- November 7, 2018
- Report Date
- November 7, 2018
- Manufacturer
- Agfa N.V.
- Product Code
- KPR
- Report Source
- Manufacturer report
- Reporter Location
- BE
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 884964 | KPR |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |