FDA Adverse Event No answer provided Summary report: N

COR22000043-000

MDR report key: 13636543 · Received February 28, 2022

Report

Report Number
COR22000043-000
Event Type
No answer provided
Date Received
February 28, 2022
Report Date
February 28, 2022
Product Code
EAP
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1778348 EAP

Patients

Seq Age Sex Outcome Treatment
1