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

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    K-ASSAY MULTI-ANALYTE CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    FORCEPS CEV405 FENESTRATED 350MM JOHANN [MXI/XOM]

    FDA Adverse Event
    Injury ·XOMED MICROFRANCE MFG·Product code GEI·March 19, 2014

    COULTER CLONE T8 MONOCLONAL ANTIBODY

    FDA 510(k)
    FDA Class 2 ·Hematology

    SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 8, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 11, 2011

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWP·August 8, 2014