FDA Adverse Event
Other
Summary report: N
COR19000248-000
MDR report key: 8577679
·
Received May 2, 2019
Report
- Report Number
- COR19000248-000
- Event Type
- Other
- Date Received
- May 2, 2019
- Report Date
- May 2, 2019
- 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 |
|---|---|---|---|---|---|---|---|
| 365141 | KPR |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |