BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    COMFIT BLUE POWDERED EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SeaSpine Spacer System - Redondo™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981045494·Redondo Trial 34mm x 24mm x 18mm, 8 Deg

    MODIFICATIONS TO INTRA-AORTIC BALLOONS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    URETERAL COMPRESSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 30, 2013

    PENTA LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·SJM NEUROMODULATION DIV.·Product code LGW·December 14, 2010

    UNKNOWN DEPUY HIP STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KXA·July 15, 2014