220 results · 43ms · Sources: EU EUDAMED, US FDA

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EKOS CORPORATION

FDA Adverse Event
Injury ·EKOS CORPORATION·Product code KRA·December 9, 2013

EKOSONIC ENDOVASCULAR CATHETER

FDA Adverse Event
Malfunction ·EKOS CORP.·Product code KRA·November 17, 2015

EKOSONIC ENDOVASCULAR CATHETER

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·May 7, 2018

EKOSONIC ENDOVASCULAR CATHETER

FDA Adverse Event
Injury ·EKOS CORPORATION·Product code KRA·December 18, 2017

EKOSONIC ENDOVASCULAR CATHETER

FDA Adverse Event
Injury ·EKOS CORPORATION·Product code KRA·December 15, 2017

EKOSONIC KIT 106CM 40CM TZ

FDA Adverse Event
Injury ·EKOS CORPORATION·Product code KRA·May 13, 2021

EKOSONIC KIT 135CM 50CM TZ

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·April 23, 2021

CATHETER, CONTINUOUS FLUSH

FDA Adverse Event
Injury ·EKOS CORPORATION·Product code KRA·May 13, 2021

EKOSONIC ENDOVASCULAR CATHETER

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·October 9, 2017

EKOSONIC ENDOVASCULAR CATHETER

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·October 23, 2017

EKOSONIC KIT 135CM 50CM TZ

FDA Adverse Event
Injury ·EKOS CORPORATION·Product code KRA·April 19, 2021

EKOSONIC KIT 106CM 12CM TZ

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·June 11, 2021

EKOSONIC ENDOVASCULAR SYSTEM

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·April 6, 2012

EKOSONIC ENDOVASCULAR SYSTEM

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·April 6, 2012

EKOSONIC ENDOVASCULAR SYSTEM

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·April 6, 2012

EKOSONIC ENDOVASCULAR SYSTEM

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·February 2, 2012

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FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·January 9, 2012

EKOSONIC

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·November 15, 2017

EKOSONIC ENDOVASCULAR CATHETER

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code KRA·December 15, 2017

LYSUS INFUSION CATHETER

FDA Adverse Event
Malfunction ·EKOS CORPORATION·Product code NUI·April 11, 2007