FDA Adverse Event Injury Summary report: N

2022588-1998-00001

MDR report key: 183879 · Received August 18, 1998

Report

Report Number
2022588-1998-00001
Event Type
Injury
Date Received
August 18, 1998
Date of Event
June 15, 1998
Product Code
DSI
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1