FDA Adverse Event No answer provided Summary report: N

COR24000344-000

MDR report key: 20967155 · Received December 18, 2024

Report

Report Number
COR24000344-000
Event Type
No answer provided
Date Received
December 18, 2024
Report Date
December 18, 2024
Product Code
GEX
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2155708 GEX
2376925 REG

Patients

Seq Age Sex Outcome Treatment
1 NA