8 results
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34ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD VERITOR ¿ SARS-COV-2 & FLU A+B
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QMN·August 3, 2022
BD VERITOR ¿ SARS-COV-2 & FLU A+B
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QMN·March 2, 2022
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·September 10, 2025
BD VERITOR ¿ SARS-COV-2 & FLU A+B
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QMN·March 2, 2022
PERSONA PEGGED POROUS TIBIAL PLATE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code OIY·November 12, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·September 19, 2011
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·July 29, 2013
BD VERITOR ¿ SARS-COV-2 & FLU A+B
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QMN·February 14, 2022