FDA Adverse Event Other Summary report: N

COR23000041-000

MDR report key: 16514236 · Received March 9, 2023

Report

Report Number
COR23000041-000
Event Type
Other
Date Received
March 9, 2023
Report Date
March 9, 2023
Manufacturer
Candela Corporation
Product Code
GEX
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
716147 GEX

Patients

Seq Age Sex Outcome Treatment
1 Other