FDA Adverse Event Other Summary report: N

COR16000124-000

MDR report key: 5567740 · Received April 11, 2016

Report

Report Number
COR16000124-000
Event Type
Other
Date Received
April 11, 2016
Report Date
April 7, 2016
Product Code
RCG
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
222033 RCG

Patients

Seq Age Sex Outcome Treatment
1