38 results · 36ms · Sources: EU EUDAMED, US FDA

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PENUMBRA SYSTEM REPERFUSION CATHETER 026

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code DQY·February 9, 2010

PENUMBRA SYSTEM

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code NRY·June 25, 2010

PENUMBRA SYS CATHETER 026/NEURON CATHETER 053

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code NRY·April 16, 2010

PENUMBRA SYSTEM

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code NRY·April 16, 2010

PENUMBRA SYSTEM REPERFUSION CATHETER 041

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code NRY·April 16, 2010

PENUMBRA STROKE SYSTEM

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code DQY·April 9, 2010

PENUMBRA SYSTEM REPERFUSION CATHETER 054

FDA Adverse Event
Other ·PENUMBRA INC.·Product code NRY·October 26, 2010

PENUMBRA SYSTEM SEPARATOR 032

FDA Adverse Event
Other ·PENUMBRA INC.·Product code NRY·October 26, 2010

PENUMBRA SYSTEM SEPARATOR 032

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code NRY·October 26, 2010

032 SEPARATOR

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code NRY·November 17, 2009

032 REPERFUSION CATHETER

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code NRY·November 13, 2009

NEURON DELIVERY CATHETER 070 ADVANCED

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code DQY·October 13, 2009

032 REPERFUSION CATHETER

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code NRY·November 17, 2009

032 SEPARATOR

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code DQY·November 17, 2009

PENUMBRA SYSTEM REPERFUSION CATHETER 032

FDA Adverse Event
Other ·PENUMBRA INC.·Product code NRY·October 26, 2010

PENUMBRA SYSTEM SEPARATOR 054

FDA Adverse Event
Other ·PENUMBRA INC.·Product code NRY·October 26, 2010

PENUMBRA SYSTEM

FDA Adverse Event
Other ·PENUMBRA INC.·Product code NRY·February 3, 2011

NEURON DELIVERY CATHETER 070

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code DQY·September 29, 2009

NEURON SELECT CATHETER 053

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code DQY·September 30, 2009

NEURON DELIVERY CATHETER 070

FDA Adverse Event
Other ·PENUMBRA, INC.·Product code DQY·September 30, 2009