FDA Adverse Event Death Summary report: N

*

MDR report key: 566895 · Received January 17, 2005

Report

Report Number
2022870-2005-00001
Event Type
Death
Date Received
January 17, 2005
Date of Event
December 6, 2004
Manufacturer
MEDICAL DATA ELECTRONICS
Product Code
DRT
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
RISK MANAGER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * DRT MEDICAL DATA ELECTRONICS * *

Patients

Seq Age Sex Outcome Treatment
1 * Death VENTILATOR