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·January 10, 2014
ZELTIQ EZ APP 8.0
FDA Adverse Event
Injury
·ZELTIQ AESTHETICS, INC.·Product code OOK·October 12, 2012
SPRINT FIDELIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 10, 2010