FDA Adverse Event Other Summary report: N

COR24000069-000

MDR report key: 19163581 · Received April 23, 2024

Report

Report Number
COR24000069-000
Event Type
Other
Date Received
April 23, 2024
Report Date
April 22, 2024
Product Code
MKB
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
1189615 MKB

Patients

Seq Age Sex Outcome Treatment
1 NA Other