BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    MAGNISCAN 5000 MR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRUST DAM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ePM Series Patient monitors

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TEGO¿ CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·January 25, 2023

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES IRELAND LTD.·Product code HQL·June 10, 2014

    THERMOCHOICE III

    FDA Adverse Event
    Malfunction ·GYNECARE WORLDWIDE DIVISION OF ETHICON INC·Product code MKN·October 22, 2010

    S3 EX - 3005

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·November 29, 2012