FDA Adverse Event Other Summary report: N

COR19000055-000

MDR report key: 8271200 · Received January 23, 2019

Report

Report Number
COR19000055-000
Event Type
Other
Date Received
January 23, 2019
Report Date
January 23, 2019
Manufacturer
Agfa N.V.
Product Code
JAA
Report Source
Manufacturer report
Reporter Location
BE
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
62480 JAA

Patients

Seq Age Sex Outcome Treatment
1 NA Other