BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M2A-MAGNUM MOD HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 20, 2020

    M2A-MAGNUM RECAP CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 20, 2020

    M2A-MAGNUM 42-50 TAPER INSRT STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 20, 2020

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·January 27, 2011

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 19, 2013

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·March 4, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LFR·March 11, 2008