6 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DEPTH ELECTRODE
FDA Adverse Event
Malfunction
·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·December 14, 2021
SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS
FDA Adverse Event
Injury
·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 30, 2014
PUMP IN STYLE
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·December 17, 2010
ACTIVA
FDA Adverse Event
Malfunction
·NEURO - VILLALBA·Product code MHY·February 15, 2013
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·February 6, 2017