FDA Adverse Event No answer provided Summary report: N

COR26000101-000

MDR report key: 25008327 · Received April 27, 2026

Report

Report Number
COR26000101-000
Event Type
No answer provided
Date Received
April 27, 2026
Report Date
April 27, 2026
Product Code
GEX
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1054966 GEX

Patients

Seq Age Sex Outcome Treatment
1 NA