FDA Adverse Event No answer provided Summary report: N

COR24000031-000

MDR report key: 18758567 · Received February 22, 2024

Report

Report Number
COR24000031-000
Event Type
No answer provided
Date Received
February 22, 2024
Report Date
February 18, 2024
Product Code
GEX
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
46 GEX

Patients

Seq Age Sex Outcome Treatment
1 NA