BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PINN SECTOR HA ACET CUP 50MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·May 9, 2014

    ZMR FEMORAL STEM

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code LPH·October 19, 2012

    EEA 31MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·August 11, 2010