BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    COAGUCHEK SYSTEM, COAGUCHEK SYSTEM FOR PROTHROMBIN TIME SELF TESTING

    FDA 510(k)
    FDA Class 2 ·Hematology

    SUREDROP EYEDROP GUIDE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    EMIT(R) II 9 CANNABINOID NEGATIVE CALIBRA/CONTROLS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·January 17, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI, INC.·Product code EGS·May 12, 2015

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·October 9, 2025

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·December 19, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·March 1, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·January 15, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·June 6, 2018

    DA-800C5L

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·May 2, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018