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

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    MODIFIED QUINTON SINGLE LUMEN CATHETER

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

    UROLOGICAL LOOP RETRIEVERS

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

    BONE CURETTE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 16, 2014

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 12

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·December 28, 2012