FDA Adverse Event No answer provided Summary report: N

COR24000159-000

MDR report key: 19910639 · Received August 5, 2024

Report

Report Number
COR24000159-000
Event Type
No answer provided
Date Received
August 5, 2024
Report Date
August 5, 2024
Product Code
RFN
Report Source
Manufacturer report
Reporter Location
Gu, CH
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1025736 RFN

Patients

Seq Age Sex Outcome Treatment
1 NA