4 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
NAVITOR TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code NPT·February 16, 2024
HYPODERMIC NEEDLE-PRO AND NEEDLE WITH NEEDLE PROTECTION DEVICE
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FMJ·February 4, 2013
ASR UNI FEMORAL IMPL SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 31, 2011
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON MANUFACTURING, LTD.·Product code HQC·July 2, 2014