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

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    Filters FDA Adverse Event ×

    MICROSPAN SYSTEM

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code FED·June 8, 2006

    ASR ACETABULAR IMPLANT 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 14, 2013

    REPLACEMENT HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·January 14, 2011

    CODMAN LUMBAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF·Product code JXG·July 28, 2014

    PFCSIGMA POST FEM AUG TRL4MMS5

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWT·April 29, 2022

    FLEXOR PARALLEL URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Injury ·COOK INC·Product code EZN·May 21, 2019