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

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    HISTO-CHECK LEGIONELLA CONTROL SLIDES

    FDA 510(k)
    FDA Class 1 ·Microbiology

    GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Vyntus/SentrySuite Product Line

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    6461500 INFUSOR PUMP (1 LABEL)

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 11, 2010

    INOGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 1, 2015

    GYNECARE MESH UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 19, 2014

    TI MATRIX LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·December 21, 2012