FDA Adverse Event No answer provided Summary report: N

COR18000148-000

MDR report key: 7503649 · Received February 12, 2018

Report

Report Number
COR18000148-000
Event Type
No answer provided
Date Received
February 12, 2018
Report Date
February 5, 2018
Product Code
RFZ
Report Source
Manufacturer report
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
106015 RFZ

Patients

Seq Age Sex Outcome Treatment
1