4 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 9, 2014
KEEPSAFE FALL MONITOR
FDA Adverse Event
Malfunction
·DONGGUAN POSEY MEDICAL DEVICE LTD.·Product code KMI·November 3, 2010
OBTAPE TRANSOBTURATOR SLING
FDA Adverse Event
Injury
·MENTOR WORLDWIDE LLC·Product code FTL·December 21, 2012
GYC-1000
FDA Adverse Event
Malfunction
·NIDEK CO., LTD.·Product code HQF·June 18, 2015