FDA Adverse Event Other Summary report: N

COR18001629-000

MDR report key: 7953907 · Received October 10, 2018

Report

Report Number
COR18001629-000
Event Type
Other
Date Received
October 10, 2018
Report Date
October 10, 2018
Manufacturer
Lumenis Ltd.
Product Code
EWG
Report Source
Manufacturer report
Reporter Location
IS
Reporter Occupation
OTHER
Health Professional
I

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
791079 EWG

Patients

Seq Age Sex Outcome Treatment
1 Other