832 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ZINGER GUIDE WIRE - CRDM
FDA Adverse Event
Injury
·MEDTRONIC, INC·Product code DQT·August 4, 2015
HI-PER COAT DIRECT WIRE 300ST
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DQT·February 2, 2004
HI-PER COAT DIRECT WIRE 300ST
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DQT·February 2, 2004
ZINGER GUIDE WIRE - CRDM
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DQT·April 11, 2014
PRUITT IRRIGATION OCCLUSION CATHETER
FDA Adverse Event
Malfunction
·IDEAS FOR MEDICINE, INC.·Product code DQT·September 6, 1996
PRUITT IRRIGATION OCCLUSION CATHETER
FDA Adverse Event
Malfunction
·IDEAS FOR MEDICINE, INC.·Product code DQT·September 6, 1996
HI-PER COAT DIRECT WIRE 300ST
FDA Adverse Event
MEDTRONIC, INC.·Product code DQT·February 2, 2004
AGA
FDA Adverse Event
Injury
·AGA MEDICAL CORP.·Product code DQT·February 3, 2004
HI-PER COAT DIRECT WIRE 300ST
FDA Adverse Event
Malfunction
·MEDTRONIC INC.·Product code DQT·March 16, 2004
HI-PER COAT DIRECT WIRE 300CM
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DQT·March 4, 2004
ZINGER MEDIUM
FDA Adverse Event
Injury
·MEDTRONIC, INC·Product code DQT·April 11, 2014
ZINGER GUIDE WIRE - CRDM
FDA Adverse Event
Malfunction
·MEDTRONIC, INC·Product code DQT·December 7, 2017
COMMODORE
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR·Product code DQT·March 20, 2002
PRUITT AORTIC OCCLUSION CATHETER
FDA Adverse Event
Death
·LEMAITRE VASCULAR·Product code DQT·January 12, 2012
HI-PER COAT DIRECT WIRE 300ST
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DQT·December 22, 2003
HI-PER COAT DIRECT WIRE 300ST
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DQT·December 15, 2003
HI-PER COAT DIRECT WIRE 300CM STRAIGHT
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DQT·November 10, 2003
OCCLUSION BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code DQT·September 4, 2003
MEDI-TECH
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP·Product code DQT·July 15, 2003
OCCLUSION BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code DQT·September 4, 2003