BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    SENTINEL SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036028886·

    NAC Y-ADP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BMR DENTAL IMPLANT SYSTEM, MODEL 3.3XX, EITHER HA OR TPS COATED, 3.308, 3.310,3.312, 3.314 3.316

    FDA 510(k)
    FDA Class 2 ·Dental

    M2A-MAGNUM PF CUP 52ODX46ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 2, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 16, 2011

    UNKNOWN DEPUY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·July 30, 2008