6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MEVATRON KD-2
FDA Adverse Event
Malfunction
·SIEMENS MEDICAL SOLUTIONS OCS·Product code IYE·December 12, 2007
ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)
FDA Adverse Event
Injury
·ANGIOSCORE, INC·Product code LIT·March 29, 2016
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2014
TRI-LOCK BPS SZ 9 HI OFFSET
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 7, 2012
DXTEND SCREW LOCK D4.5X36MM
FDA Adverse Event
Injury
·DEPUY FRANCE S.A.·Product code HSD·August 27, 2010
ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)
FDA Adverse Event
Malfunction
·ANGIOSCORE, INC·Product code LIT·November 26, 2015