FDA Adverse Event No answer provided Summary report: N

COR19000011-000

MDR report key: 8214730 · Received January 3, 2019

Report

Report Number
COR19000011-000
Event Type
No answer provided
Date Received
January 3, 2019
Report Date
January 3, 2019
Product Code
EHB
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
3989 EHB

Patients

Seq Age Sex Outcome Treatment
1