FDA Adverse Event Other Summary report: N

COR15000419-000

MDR report key: 5086403 · Received September 18, 2015

Report

Report Number
COR15000419-000
Event Type
Other
Date Received
September 18, 2015
Report Date
September 16, 2015
Product Code
RIF
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
617463 RIF

Patients

Seq Age Sex Outcome Treatment
1