FDA Adverse Event Other Summary report: N

COR20000031-000

MDR report key: 9612448 · Received January 20, 2020

Report

Report Number
COR20000031-000
Event Type
Other
Date Received
January 20, 2020
Report Date
January 20, 2020
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
68071 KPR

Patients

Seq Age Sex Outcome Treatment
1 Other