BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·March 31, 2016

    RAD-8

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·July 15, 2015

    RHYTHMIA HDX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025

    CONSERVE(R) SF CEMENTED FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code KXA·October 22, 2014

    SROM MAR LNR M 28MM+3MM 10 DEG

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code KWA·June 27, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 25, 2011