10 results
·
38ms
·
Sources: EU EUDAMED, US FDA
EUROMI S.A.
FDA registration
EUROMI S.A.·2 products·🇧🇪 Belgium
EUROMI REUSABLE CANNULA
FDA Adverse Event
Injury
·EUROMI SA·Product code GEA·June 23, 2023
EUROMI REUSABLE CANNULA
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·June 27, 2023
CANULE VITERBO 3*250 MM TUNGSTÈNE
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·April 14, 2023
CANNULA
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·April 17, 2023
CANNULA
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·April 17, 2023
REBELO 5*350 TITANIUM
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·June 28, 2023
EVAMATIC
FDA Adverse Event
Injury
·EUROMI SA·Product code QPB·June 28, 2023
CANNULAS
FDA Adverse Event
Malfunction
·EUROMI SA·Product code GEA·November 8, 2024
CMC Medical Devices & Drugs SL
Authorized representative
🇪🇸 Spain·698 Manufacturers·11260 Devices