43 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·December 11, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·October 31, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMS·Product code GEX·October 18, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMS·Product code GEX·October 18, 2012
LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code LDD·December 4, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMS·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMS·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS·Product code GEX·October 22, 2012
AMS GREENLIGH HPS FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·February 12, 2013
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Injury
·AMERICAN MED SYSTEMS·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Malfunction
·AMS·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code GEX·October 22, 2012
AMS GREENLIGHT HPS FIBER
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS·Product code GEX·October 22, 2012
AMS GREENLIGT HPS FIBER
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS·Product code GEX·October 22, 2012
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
ANI [ A&I ] GROUP TAIWAN·Product code IOR·April 16, 2013
QUANTUM TTC ESOPHAGEAL BALLOON DILATOR
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC·Product code KNQ·March 17, 2011