BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

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    ALL SILICONE INTERMITTENT CATHETER

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

    CHLOE BLAST

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BODYSCREEN II

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FOUNDATION KNEE

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code JWH·December 22, 2010

    ALTRX +4 NEUT 36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·February 5, 2013

    ELLIPSE DR, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 18, 2014