16 results
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93ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ALTAIRE
FDA Adverse Event
Injury
·HITACHI MEDICAL CORP.·Product code LNH·March 23, 2005
AIRIS
FDA Adverse Event
Injury
·HITACHI MEDICAL CORP.·Product code LNH·March 23, 2005
NOBLUS
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code IYN·March 8, 2022
PROSOUND F-75
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code IYN·March 8, 2022
ALTAIRE MR SYSTEM
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code LNH·March 8, 2022
ECHELON OVAL
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code LNH·March 8, 2022
AIRIS ELITE MR SYSTEM
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code LNH·March 8, 2022
CV41 PROBE
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code IYN·March 8, 2022
AIRIS ELITE MR SYSTEM
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code LNH·March 8, 2022
AIRIS II MRI SYSTEM
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code LNH·March 8, 2022
AIRIS ELITE
FDA Adverse Event
Malfunction
·HITACHI MEDICAL CORPORATION·Product code LNH·July 2, 2014
HITACHI ALTAIRE HIGH-FIELD PERFORMANCE
FDA Adverse Event
Other
·HITACHI MEDICAL SYSTEMS AMERICA, INC.·Product code LNH·December 12, 2003
AIRIS II MRI SCANNER
FDA Adverse Event
Malfunction
·HITACHI MEDICAL SYSTEMS AMERICA, INC·Product code LNH·July 25, 2014
OASIS HIGH-FIELD BORE-LESS MR
FDA Adverse Event
HITACHI MEDICAL SYSTEMS AMERICA, INC.·Product code LNI·January 7, 2015
HITACHI AIRIS 2 SYSTEM
FDA Adverse Event
Other
·HITACHI MEDICAL SYSTEMS AMERICA, INC.·Product code LNH·March 29, 1999
ARIETTA 850
FDA Adverse Event
Injury
·FUJIFILM HEALTHCARE CORPORATION·Product code IYN·March 8, 2022