6 results
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44ms
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Sources: EU EUDAMED, US FDA
STELLANT
FDA Adverse Event
MEDRAD, INC.·Product code DXT·August 7, 2006
STELLANT
FDA Adverse Event
MEDRAD, INC.·Product code DXT·August 7, 2006
STELLANT
FDA Adverse Event
MEDRAD, INC.·Product code DXT·August 7, 2006
Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. The user, responsible to interpret the monitored data made available, will be a professional healthcare provider. Physiological data, gas monitoring, system alarms, and patient analysis will be available to the care provider from the monitor.
FDA Recall
Terminated
·Medrad Mr Inc·Product code MWI·November 21, 2013
Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. The user, responsible to interpret the monitored data made available, will be a professional healthcare provider. Physiological data, gas monitoring, system alarms, and patient analysis will be available to the care provider from the monitor.
FDA Enforcement
Class II
·Terminated·Medrad Mr Inc·January 29, 2014
DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor, Physiological, Patient
FDA Recall
Terminated
·Medrad Inc·Product code MWI·April 15, 2013