BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    VedDilator ^TM (3-Stage Balloon Dilation Catheter)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NA

    FDA UDI
    DEPUY MITEK, LLC·10886705011070·LIGAMENT GRAFT PASSER/PROTECTOR 8.5mm

    AJAX DENTAL UNIT

    FDA 510(k)
    FDA Class 1 ·Dental

    ARTHREX FIBERTAPE (TM), 2MM, ARTHREX FIBERTAPE (TM), 3MM, ARTHREX FIBERTAPE (TM), 4MM, MODELS AR-7237, AR-7238, AR-7239

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

    N/A

    FDA UDI
    Exactech, Inc.·10885862660022·Trial, Monobloc Revision Stem

    NA

    FDA UDI
    Exactech, Inc.·10885862282903·TRIAL, MONOBLOC REVISION STEM, 23x245mm

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·November 13, 2008

    PULSE GEN MODEL 103

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 2, 2011

    CARESITE (LAD)

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL, INC.·Product code FPA·July 8, 2013

    COPAN WASP/COLIBRI

    FDA Adverse Event
    Other ·COPAN WASP·Product code QQV·July 25, 2024