3 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·June 6, 2014
CANNULATED SCREW
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·December 3, 2012
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·September 3, 2010