FDA Adverse Event Other Summary report: N

COR20000272-000

MDR report key: 10771585 · Received November 1, 2020

Report

Report Number
COR20000272-000
Event Type
Other
Date Received
November 1, 2020
Report Date
November 1, 2020
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
1232419 GEX

Patients

Seq Age Sex Outcome Treatment
1 Other