BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

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    ACUMED SUTURE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131261717·H10, BTE 13 WL 85 STG

    GENESIS VERTICAL PLATFORM LIFT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    STOCKERT AIR PURGE CONTROL SYSTEM MODEL 23-45-05

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ATTAIN ABILITY

    FDA Adverse Event
    Death ·MPRI·Product code OJX·May 29, 2013

    MOOG CURLIN INFUSION

    FDA Adverse Event
    Other ·MOOG MEDICAL SERVICES GROUP·Product code LZH·June 14, 2011

    HEMOSTATIC CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MND·August 22, 2008