FDA Adverse Event No answer provided Summary report: N

COR22000054-000

MDR report key: 13760718 · Received March 14, 2022

Report

Report Number
COR22000054-000
Event Type
No answer provided
Date Received
March 14, 2022
Report Date
March 14, 2022
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
46967 MKB

Patients

Seq Age Sex Outcome Treatment
1