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

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    SIGMA DIAGNOSTICS ELECTROLYTE BUFFER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    RADIOLUCENT INSERTION HANDLE FRN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HSB·March 8, 2023

    EM II DISPOSABLE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIPAP AUTOSV

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PLUM A+ W/MEDNET RE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 30, 2014

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 15, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 20, 2010

    BA102

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·March 31, 2016

    BA105

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·March 28, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·August 29, 2017

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015