FDA Adverse Event No answer provided Summary report: N

COR22000267-000

MDR report key: 16052448 · Received December 27, 2022

Report

Report Number
COR22000267-000
Event Type
No answer provided
Date Received
December 27, 2022
Report Date
December 23, 2022
Product Code
RHP
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2653610 RHP

Patients

Seq Age Sex Outcome Treatment
1 NA