FDA Adverse Event No answer provided Summary report: N

COR21000128-000

MDR report key: 11760327 · Received April 30, 2021

Report

Report Number
COR21000128-000
Event Type
No answer provided
Date Received
April 30, 2021
Report Date
April 29, 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
647221 OWB

Patients

Seq Age Sex Outcome Treatment
1