9 results
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30ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BAXANO IO-FLEX SYSTEM
FDA Adverse Event
Other
·BAXANO, INC.·Product code HAE·July 2, 2012
BAXANO IO-FLEX SYSTEM
FDA Adverse Event
Other
·BAXANO, INC.·Product code HAE·July 2, 2012
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 15, 2021
BAXANO IO-FLEX SYSTEM
FDA Adverse Event
Other
·BAXANO, INC.·Product code HAE·July 2, 2012
OPRA IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·INTEGRUM AB·Product code PJY·December 8, 2023
ARTERIAL CANNULA
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code DWF·March 15, 2013
CRYSTALENS
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·March 4, 2011
AV PLUS DX BIFURCATED BIPOLAR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2008
TOTAL ASR ACET IMP SIZE 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD.·Product code KWA·June 12, 2013