BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COBAS 8000 C 702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 24, 2024

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·April 18, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·September 20, 2012

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIVISION·Product code FPO·July 12, 2010

    6.0MM TI HARD ROD 350MM

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code NKB·February 1, 2017

    TI CLICK'X® LOCKING CAP FOR TI 3-D HEAD

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code NKB·February 1, 2017