3 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
RELIEVA SINUS BALLOON CATHETER SYSTEM
FDA Adverse Event
Injury
·ACCLARENT, INC.·Product code KAM·April 11, 2014
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 19, 2007
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 26, 2012