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

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    Filters FDA Adverse Event ×

    LEGACY 3 IMPLANT

    FDA Adverse Event
    Injury ·IMPLANT DIRECT SYBRON MANUFACTURING LLC·Product code DZE·October 3, 2019

    MK SYRINGE 3-P, LL 10CC

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FMF·May 29, 2014

    MINIARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·November 29, 2012

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·September 30, 2010