3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 6, 2013
SURGICAL STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM DE MEXICO S DE RL DE CV·Product code FPO·January 13, 2011
MITEK OMNISPAN MENISCAL REPAIR SYSTEM, 27 DEGREE
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MBI·July 31, 2014