10 results
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32ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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DUO EXTEND VENOUS STENT SYSTEM
FDA Adverse Event
Injury
·VESPER MEDICAL INC.·Product code QAN·August 1, 2024
DUO EXTEND VENOUS STENT SYSTEM
FDA Adverse Event
Malfunction
·VESPER MEDICAL INC.·Product code QAN·July 31, 2024
DUO EXTEND VENOUS STENT SYSTEM
FDA Adverse Event
Injury
·VESPER MEDICAL INC.·Product code QAN·July 31, 2024
DUO EXTEND VENOUS STENT SYSTEM
FDA Adverse Event
Malfunction
·VESPER MEDICAL INC.·Product code QAN·August 1, 2024
DUO HYBRID VENOUS STENT SYSTEM
FDA Adverse Event
Malfunction
·VESPER MEDICAL INC.·Product code QAN·August 1, 2024
RESONANT LIGHT, INC. OF B.C., CANADA
FDA Adverse Event
Other
·RESONANT LIGHT TECHNOLOGY INC.·Product code LDQ·October 25, 2002
EZ STEER¿ THERMOCOOL® NAV BI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code OAD·September 11, 2018
PROLENE* POLYPROPYLENE MESH
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·July 31, 2025
PULSE GEN MODEL 1000
FDA Adverse Event
Injury
·LIVANOVA USA, INC.·Product code LYJ·March 14, 2025
GORE® EXCLUDER® CONFORMABLE AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·September 26, 2024