BEUDAMED
    14 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SCHILLER

    FDA Adverse Event
    Malfunction ·SCHILLER AG·Product code MHX·November 2, 2006

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    DISC LT DSTL HMRL BDY SET

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 1, 2013

    ACCU-CHEK FLEXLINK PLUS

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FRN·March 4, 2011

    IN SITU BENDER-RIGHT

    FDA Adverse Event
    Malfunction ·SYNTHES TUTTLINGEN·Product code HXP·August 15, 2014

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    INTELLIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·June 28, 2018