220 results
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43ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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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
*
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