FDA Adverse Event Other Summary report: N

COR15000344-000

MDR report key: 4987492 · Received August 8, 2015

Report

Report Number
COR15000344-000
Event Type
Other
Date Received
August 8, 2015
Report Date
August 8, 2015
Product Code
RBJ
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
521174 RBJ

Patients

Seq Age Sex Outcome Treatment
1