FDA Adverse Event Other Summary report: N

COR19000402-000

MDR report key: 8983981 · Received September 9, 2019

Report

Report Number
COR19000402-000
Event Type
Other
Date Received
September 9, 2019
Report Date
September 9, 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
767276 KPR

Patients

Seq Age Sex Outcome Treatment
1 Other