BEUDAMED
    9 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ASCENT CLSD BOX PS FMRL LG R

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 25, 2017

    18X150 ASCENT FML POROUS STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 3, 2017

    PHOENIX 3.5MM INSERTER SHORT

    FDA Adverse Event
    Injury ·BIOMET TRAUMA·Product code HXX·August 8, 2017

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·August 16, 2013

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 2, 2014

    PORTEX 9.0MM VOCALAID TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD, INC.·Product code CAZ·October 25, 2012

    PUMP MMT-522CAL PRDGM INS V2.2 CL EN PR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·September 10, 2010

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·August 16, 2013

    PHOENIX 3.5MM INSERTER CONNECTOR SHORT

    FDA Adverse Event
    Injury ·BIOMET TRAUMA·Product code LXH·August 8, 2017