FDA Adverse Event Other Summary report: N

COR14000036-000

MDR report key: 3595056 · Received January 28, 2014

Report

Report Number
COR14000036-000
Event Type
Other
Date Received
January 28, 2014
Report Date
January 28, 2014
Product Code
RBY
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
60142 RBY

Patients

Seq Age Sex Outcome Treatment
1