FDA Adverse Event No answer provided Summary report: N

COR25000044-000

MDR report key: 21268060 · Received January 29, 2025

Report

Report Number
COR25000044-000
Event Type
No answer provided
Date Received
January 29, 2025
Report Date
January 29, 2025
Product Code
RDW
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
605973 RDW

Patients

Seq Age Sex Outcome Treatment
1 NA