3 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 4, 2014
DELTA CER HEAD 12/14 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LZO·October 23, 2012
MAGIC 3 FEMALE INTERMITTENT CATHETER
FDA Adverse Event
Malfunction
·ROCHESTER MEDICAL CORP·Product code KOD·May 27, 2015