FDA Adverse Event Other Summary report: N

COR16000386-000

MDR report key: 5885860 · Received August 18, 2016

Report

Report Number
COR16000386-000
Event Type
Other
Date Received
August 18, 2016
Report Date
August 5, 2016
Product Code
REG
Report Source
Manufacturer report
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
536747 REG

Patients

Seq Age Sex Outcome Treatment
1