FDA Adverse Event Other Summary report: N

1911273-1998-00001

MDR report key: 196261 · Received November 9, 1998

Report

Report Number
1911273-1998-00001
Event Type
Other
Date Received
November 9, 1998
Date of Event
September 21, 1998
Product Code
BXB
Report Source
Manufacturer report

Devices

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

Patients

Seq Age Sex Outcome Treatment
1