BEUDAMED
    7 results · 24ms · Sources: EU EUDAMED, US FDA

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    DRE Duo

    FDA 510(k)
    FDA Class 2 ·Radiology

    t:slim Insulin Delivery System, t:flex Insulin Delivery System, Tandem Device Updater

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CYTORI CELUTION CELL CONCENTRATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MEDLINE UNITE

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, LP·Product code JDR·December 23, 2025

    SPACEMAKER BLUNT TIP TROCAR 10MM

    FDA Adverse Event
    Malfunction ·USSC PUERTO RICO·Product code GCJ·August 19, 2011

    UNKNOWN DEPUY FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. - 1818910·Product code KXA·November 18, 2014

    ARCOMXL 32MM +3 HW LNR SZ 22

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·December 2, 2015