FDA Adverse Event No answer provided Summary report: N

COR21000140-000

MDR report key: 11826467 · Received May 14, 2021

Report

Report Number
COR21000140-000
Event Type
No answer provided
Date Received
May 14, 2021
Report Date
May 14, 2021
Product Code
OWB
Report Source
Manufacturer report
Reporter Location
NL
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
720249 OWB

Patients

Seq Age Sex Outcome Treatment
1