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

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    PERCOR PERCUTANEOUS INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAGELLAN 3ML SFTY COMBO 25X1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 12, 2019

    MAGELLAN 3ML SFTY COMBO 25X1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 9, 2019

    CORPATH 200 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD INTROSYTE PRECISION INTRODUCER; BD INTROSYTE-N PRECISION INTRODUCER; BD INTROSYTE AUTOGUARD SHIELDED INTRODUCER; BD I

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 8, 2014

    GOLDEN COMFORTER

    FDA Adverse Event
    Malfunction ·GOLDEN TECHNOLOGIES, INC.·Product code INO·October 3, 2012

    MK1 POOL LIFT

    FDA Adverse Event
    Malfunction ·MEDIBO MEDICAL PRODUCTS NV·Product code FSA·June 4, 2015

    MAGELLAN 3ML SFTY COMBO 25X1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 11, 2019