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

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    Filters FDA Adverse Event ×

    IMHS CP SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HWC·November 21, 2012

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 9, 2015

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 20, 2010