FDA Adverse Event Other Summary report: N

COR22000092-000

MDR report key: 14495936 · Received May 25, 2022

Report

Report Number
COR22000092-000
Event Type
Other
Date Received
May 25, 2022
Report Date
May 25, 2022
Manufacturer
Lumenis Ltd.
Product Code
GEX
Report Source
Manufacturer report
Reporter Location
IS
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
259833 GEX

Patients

Seq Age Sex Outcome Treatment
1 Other