FDA Adverse Event Other Summary report: N

COR18001378-001

MDR report key: 7934154 · Received October 3, 2018

Report

Report Number
COR18001378-001
Event Type
Other
Date Received
October 3, 2018
Report Date
October 3, 2018
Manufacturer
Agfa Healthcare 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
769961 KPR

Patients

Seq Age Sex Outcome Treatment
1 Other