BEUDAMED
    3 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PLV-102

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·January 3, 2013

    QUATTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·October 28, 2010

    SERIES A PAT THN 34 3 PEG

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 1, 2014