BEUDAMED
    5 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COBAS 8000 C702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 17, 2025

    COBAS 8000 C702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 27, 2026

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·June 12, 2014

    COOL-TIP RF SYS 100V ENG

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·October 22, 2010

    DEPUY PINNACLE ACETABULAR CUP SYSTEM 56

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC·Product code KWA·December 17, 2012