BEUDAMED
    236 results · 23ms · Sources: EU EUDAMED, US FDA

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    REFOBACIN -PALACOS G

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TOSOH CORP.

    FDA registration
    TOSOH CORP.·63 products·🇯🇵 Japan

    ACON AMP ONE STEP AMPHETAMINE TEST STRIP, ACON AMP ONE STEP AMPHETAMINE TEST DEVICE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HI-ART SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·October 13, 2017

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·November 7, 2018

    8031673-2009-00001

    FDA Adverse Event
    Other ·Product code JJE·February 24, 2009

    8031673-2009-00002

    FDA Adverse Event
    Other ·Product code JJE·March 20, 2009

    8031673-2017-00180

    FDA Adverse Event
    Malfunction ·December 15, 2017

    8031673-2017-00113

    FDA Adverse Event
    Malfunction ·November 17, 2017

    8031673-2000-00001

    FDA Adverse Event
    Other ·Product code JJC·June 29, 2000

    8031673-2017-00046

    FDA Adverse Event
    Malfunction ·October 5, 2017

    8031673-2005-00019

    FDA Adverse Event
    Other ·Product code ---·May 17, 2005

    8031673-2005-00018

    FDA Adverse Event
    Other ·Product code ---·May 17, 2005

    8031673-2005-00015

    FDA Adverse Event
    Product code JJE·March 2, 2005

    8031673-2005-00016

    FDA Adverse Event
    Other ·Product code JJE·March 30, 2005

    8031673-2008-00001

    FDA Adverse Event
    Other ·Product code JJE·August 18, 2008

    8031673-2005-00024

    FDA Adverse Event
    Malfunction ·Product code ---·September 13, 2005

    8031673-2017-00317

    FDA Adverse Event
    Malfunction ·January 24, 2018

    8031673-2018-02807

    FDA Adverse Event
    Malfunction ·March 13, 2018