BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    3004753838-2018-080146

    FDA Adverse Event
    Malfunction ·July 20, 2018

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·August 30, 2012

    ISODUR PROSTHESIS HEAD 12/14 32MM XL

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO KG·Product code LPH·March 28, 2014

    VERCISE GENUS?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code MHY·October 21, 2025

    SYNCHROMED II

    FDA Adverse Event
    Death ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 26, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·April 6, 2011

    DUR MAR +4 NEUT LNR 36X54

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code LPH·July 18, 2008