FDA Adverse Event No answer provided Summary report: N

COR20000068-000

MDR report key: 9729599 · Received February 19, 2020

Report

Report Number
COR20000068-000
Event Type
No answer provided
Date Received
February 19, 2020
Report Date
February 19, 2020
Product Code
IZL
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
187695 IZL

Patients

Seq Age Sex Outcome Treatment
1