FDA Adverse Event Death Summary report: N

*

MDR report key: 350082 · Received September 6, 2001

Report

Report Number
2182466-2001-00001
Event Type
Death
Date Received
September 6, 2001
Date of Event
July 31, 2001
Manufacturer
BCI, INC.
Product Code
DQA
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
40464 * DQA BCI, INC.

Patients

Seq Age Sex Outcome Treatment
1