7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BONE SCREW Ø6,5 H.25MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code MBL·July 22, 2024
BONE WAX 24X2.5G
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code MTJ·October 30, 2019
MIS CANNULATED POLYAXIAL SCREW 6X45MM,TI
FDA Adverse Event
Malfunction
·DEPUY SYNTHES SPINE·Product code NKB·June 27, 2014
VASOVIEW HEMOPRO 2 EVH SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·October 22, 2010
AUTOPULSE NIMH BATTERY
FDA Adverse Event
Malfunction
·ZOLL CIRCULATION, INC.·Product code DRM·December 26, 2012
BONE WAX 24X2.5G
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code MTJ·May 7, 2019
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 15, 2016