97 results
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32ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
POLARIS ADJUSTABLE VALVE/ANTECHAMBER 10-140
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·May 20, 2014
POLARIS
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·November 30, 2017
PARENCHYMAL PRESSIO CATHETER
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code GWM·November 14, 2017
PARENCHYMAL PRESSIO CATHETER
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code GWM·December 19, 2017
PARENCHYMAL PRESSIO CATHETER
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code GWM·October 6, 2017
SOPHY
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·November 24, 2017
POLARIS SPV KIT PREATTACHED/BO19-10
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·February 13, 2013
POLARIS SPVB KIT PREATTACHED/BO19-10
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·February 13, 2013
POLARIS SPV ADJUSTABLE VALVE/BURR HOLE
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·February 13, 2013
POLARIS SPV ADJUSTABLE VALVE/BURR HOLE
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·February 13, 2013
POLARIS VALVE
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·October 17, 2018
POLARIS ADJUSTABLE VALVE/5 PRESS
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·February 13, 2013
POLARIS ADJUSTABLE VALVE/5 PRESS.
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·May 22, 2013
SOPHY SM8 PROG. VALVE / ANTECHAMBER
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·May 22, 2013
POLARIS ADJUSTABLE VALVE/5 PRESS.
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·May 22, 2013
POLARIS SPV ADJUSTABLE VALVE/ANTICHAMBER
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·May 22, 2013
SOPHY SM8A KIT PREATTACHED / BO19-10
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code JXG·May 22, 2013
VENTRICULAR PRESSIO CATHETER
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code GWM·October 5, 2018
PRESSIO® ICP MONITORING KIT, VENTRICULAR TUNNELING
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code GWM·June 17, 2024
PARENCHYMAL PRESSIO CATHETER
FDA Adverse Event
Malfunction
·SOPHYSA SA·Product code GWM·February 13, 2017