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

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    CARETEX ISOLUTION GOWNS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CHEMSPOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RELIABLE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 17, 2025

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 10, 2014

    BILIARY STENT, BILIARY STENT SYSTEM, BILIARY ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FGE·October 12, 2010

    HUDSON SHERIDAN/HVT ET TUBE, 6.5

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·December 6, 2012