BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    OSSIOfiber® Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Wartie Advanced Wart Remover or other proprietary name

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

    ROI FUSION RODS & PLATES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·September 16, 2022

    UNK DEPUY FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSA·December 3, 2008

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·August 12, 2011

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 29, 2013