BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    UNKNOWN BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·November 4, 2020

    XPS® BUR - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·March 9, 2017

    DRILL 3055601 SKEETER OTO-TOOL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC·Product code ERL·January 11, 2013

    XPS® BUR - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·March 8, 2017

    M2A-MAGNUM PF CUP 54ODX48ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 27, 2014

    BRILLIANCE 64

    FDA Adverse Event
    PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC.·Product code JAK·November 5, 2012

    CAPSURE SP

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·June 10, 2015