3 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2014
ARTICULEZE M HEAD 36MM +12
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·October 15, 2012
WECK HEM-O-LOK TAKEAPART ENDO APPLIER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code GDO·August 4, 2010