FDA Adverse Event No answer provided Summary report: N

COR22000067-000

MDR report key: 13999492 · Received April 4, 2022

Report

Report Number
COR22000067-000
Event Type
No answer provided
Date Received
April 4, 2022
Report Date
April 4, 2022
Product Code
RHP
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1442085 RHP

Patients

Seq Age Sex Outcome Treatment
1