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

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    Filters FDA Adverse Event ×

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 2, 2025

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·August 7, 2025

    TT BASIC HVLP TRACHEOSTOMY TUBE 7.5 MM

    FDA Adverse Event
    Malfunction ·UNOMEDICAL SDN BHD·Product code JOH·March 1, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD. (GE PRIVATE)·Product code JAA·February 8, 2011

    KAPPA 900 DR

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code DXY·August 8, 2014

    ENCOREANYWHERE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·February 17, 2016