FDA Adverse Event No answer provided Summary report: N

COR23000087-000

MDR report key: 16788486 · Received April 21, 2023

Report

Report Number
COR23000087-000
Event Type
No answer provided
Date Received
April 21, 2023
Report Date
April 4, 2023
Product Code
IZL
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1601828 IZL

Patients

Seq Age Sex Outcome Treatment
1