FDA Adverse Event Malfunction Summary report: N

MEDFUSION 2010H SYRINGE INFUSION PUMP

MDR report key: 1040910 · Received April 25, 2008

Report

Report Number
2183502-2008-00107
Event Type
Malfunction
Date Received
April 25, 2008
Manufacturer
SMITHS MEDICAL MD (FORMERLY DELTEC, INC)
Product Code
FRN
Report Source
Manufacturer report

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEDFUSION 2010H SYRINGE INFUSION PUMP SYRINGE INFUSION PUMP FRN SMITHS MEDICAL MD (FORMERLY DELTEC, INC) NA

Patients

Seq Age Sex Outcome Treatment
1