FDA Adverse Event Injury Summary report: N

2082643-1998-00170

MDR report key: 147527 · Received February 6, 1998

Report

Report Number
2082643-1998-00170
Event Type
Injury
Date Received
February 6, 1998
Date of Event
January 6, 1998
Product Code
ITI
Removal / Correction Number
NA
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1