FDA Adverse Event Injury Summary report: N

1222168-2002-00001

MDR report key: 374887 · Received January 23, 2002

Report

Report Number
1222168-2002-00001
Event Type
Injury
Date Received
January 23, 2002
Date of Event
December 13, 2001
Product Code
FDI
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FDI

Patients

Seq Age Sex Outcome Treatment
1