FDA Adverse Event Malfunction Summary report: N

NEVER TOUCH VENACURE

MDR report key: 1080696 · Received April 14, 2008

Report

Report Number
1319211-2008-00015
Event Type
Malfunction
Date Received
April 14, 2008
Manufacturer
ANGIODYNAMICS, INC.
Product Code
GEX
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NEVER TOUCH VENACURE * GEX ANGIODYNAMICS, INC. * *

Patients

Seq Age Sex Outcome Treatment
1