FDA Adverse Event No answer provided Summary report: N

COR26000005-000

MDR report key: 24078838 · Received January 14, 2026

Report

Report Number
COR26000005-000
Event Type
No answer provided
Date Received
January 14, 2026
Report Date
January 14, 2026
Product Code
RFE
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
125690 RFE

Patients

Seq Age Sex Outcome Treatment
1 NA