FDA Adverse Event No answer provided Summary report: N

COR24000275-000

MDR report key: 20525320 · Received October 24, 2024

Report

Report Number
COR24000275-000
Event Type
No answer provided
Date Received
October 24, 2024
Report Date
October 24, 2024
Product Code
IZL
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2570496 IZL

Patients

Seq Age Sex Outcome Treatment
1 NA