4 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013
WAVEON CRX
FDA Adverse Event
Injury
·SONOMA ORTHOPEDIC PRODUCTS INC.·Product code HSB·November 19, 2010
INCEPTA ICD
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LWP·July 1, 2014
GENTLECATH OTHER
FDA Adverse Event
Malfunction
·UNOMEDICAL S.R.O.·Product code KOD·December 16, 2024