6 results
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36ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
REVISION FEMORAL SYSTEM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·March 27, 2024
QUATTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 22, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·March 17, 2011
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 27, 2008
REVISION MODULAR STEM Ø16MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·June 22, 2022
ACCUVUE ADVANCE
FDA Adverse Event
Injury
·VISTAKON·Product code LPL·October 19, 2007