26 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·January 24, 2023
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·June 16, 2023
8000229
FDA Adverse Event
Malfunction
·LASER PERIPHERALS, LLC·Product code GEX·May 7, 2025
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·February 25, 2021
POLYFORM SYNTHETIC MESH
FDA Adverse Event
Injury
·PROXY BIOMEDICAL LTD.·Product code FTL·November 22, 2012
LOGIC FEMORAL PS CEM LEFT SZ 2
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 31, 2024
LOGIC TIBIA PS MOD INSRT SZ 2 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 23, 2024