BEUDAMED
    7 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TI-DBLE LEAD CORT SCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSB·August 24, 2018

    RELIANCE GENFORE WASHER

    FDA Adverse Event
    STERIS CANADA CORPORATION·Product code MEC·April 11, 2013

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 13, 2011

    PALINDROME EMERALD 23/40KIT VT

    FDA Adverse Event
    Other ·TYCO HEALTHCARE/KENDALL·Product code MPB·May 28, 2008

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·February 3, 2021

    TRI-LOCK BPS SZ 4 HI OFFSET

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KWA·November 4, 2015

    TRI-LOCK BPS SZ 7 STD OFFSET

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC·Product code KWA·November 4, 2015