FDA Adverse Event Malfunction Summary report: N

DPM 4 MONITOR

MDR report key: 3091324 · Received April 30, 2013

Report

Report Number
2221819-2013-00191
Event Type
Malfunction
Date Received
April 30, 2013
Date of Event
September 25, 2012
Report Date
April 30, 2013
Manufacturer
MINDRAY DS USA, INC.
Product Code
MHX
PMA / PMN Number
070791
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

CUSTOMER REPORTED A DPM 4 MONITOR FAILED, RESULTING IN A POSSIBLE LOSS OF PRIMARY MONITORING. NO PATIENT INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
186887 DPM 4 MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

Patients

Seq Age Sex Outcome Treatment
1