7 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO2 METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014
OLM INTRACRANIAL PRESSURE MONITORING KIT
FDA Adverse Event
Malfunction
·INTEGRA NEUROSCIENCES CA/USA·Product code GWM·November 27, 2012
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 4, 2010
COMPREHENSIVE SHOULDER SYSTEM PRIMARY MINI LENGTH SHOULDER STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·March 8, 2017
COMPREHENSIVE REVERSE SHOULDER HUMERAL TRAY WITH LOCKING RING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·April 13, 2017
COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING/STANDARD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PAO·April 13, 2017
COMPREHENSIVE SHOULDER SYSTEM PRIMARY MINI LENGTH SHOULDER STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·April 13, 2017