7 results
·
40ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD PHASEAL¿ INJECTOR LUER LOCK N35
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·May 15, 2023
EDGE INSUL. COATED BLADE
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code GEI·June 26, 2013
TARGIS SYSTEM
FDA Adverse Event
Injury
·UROLOGIX, INC.·Product code MEQ·October 22, 2008
INFUSO.R.
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011
MECTACER BIOLOX DELTA FEMORAL BALL HEAD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·August 20, 2025
BD Q-SYTE LUER ACCESS SPLIT SEPTUM
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·May 6, 2022
S.M.A.R.T. NITINOL STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·January 28, 2016