3 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·June 30, 2014
HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM
FDA Adverse Event
Injury
·NORTH AMERICAN STERILIZATION &·Product code MNB·November 17, 2010
UNKNOWN VAPR ELECTRODE
FDA Adverse Event
Injury
·DEPUY MITEK·Product code GEI·January 8, 2013