10,000 results
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59ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Huestis Medical Collimator
FDA UDI
HUESTIS MACHINE CORPORATION·00850077007286·150PBL Collimator (Huestis Part # CM-32211-QMI)
44" EXTENSION SET WITH VALVES
FDA Adverse Event
Malfunction
·QMI·Product code FPA·July 20, 1998
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS EUROPA, N.V.·Product code NIQ·November 18, 2003
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·August 4, 2004
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·August 4, 2004
MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·GUIDANT VANSCULAR INTERVENTION·Product code MAF·April 5, 2005
ANES DELY SET W/ 3 Y'S
FDA Adverse Event
Malfunction
·QMI MEDICAL, INC.·Product code CAI·May 5, 1998
RESOLUTE INTEGRITY RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·July 28, 2015
BX SONIC STENT DELIVERY SYSTEM (OUS RX)
FDA Adverse Event
Death
·CORDIS DE MEXICO·Product code MAF·November 1, 2006
BX SONIC STENT DELIVERY SYSTEM (OUS RX)
FDA Adverse Event
Death
·CORDIS MEXICO·Product code MAF·November 1, 2006
RESOLUTE INTEGRITY RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·April 28, 2017
RX ACCULINK CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·December 22, 2006
RESOLUTE INTEGRITY RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·April 28, 2017
SHOCKWAVE C2 CORONARY INTRAVASCULAR LITHOTRIPSY (IVL) CATHETER
FDA Adverse Event
Injury
·SHOCKWAVE MEDICAL, INC.·Product code QMG·September 16, 2024
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·April 7, 2011
RX ACCULINK CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·June 20, 2006
JOSTENT GRAFTMASTER
FDA Adverse Event
Death
·AV-TEMECULA-CT·Product code MAF·October 11, 2013
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·June 15, 2007
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·November 13, 2006
BX SONIC STENT DELIVERY SYSTEM (OUS RX)
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code MAF·August 10, 2007