43 results · 26ms · Sources: EU EUDAMED, US FDA

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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