FDA Adverse Event No answer provided Summary report: N

COR20000080-000

MDR report key: 9813605 · Received March 10, 2020

Report

Report Number
COR20000080-000
Event Type
No answer provided
Date Received
March 10, 2020
Report Date
March 10, 2020
Product Code
IZO
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
272725 IZO

Patients

Seq Age Sex Outcome Treatment
1