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

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    CULTURE MEDIA, SELECTIVE & DIFFERENTIAL

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MAGELLAN 25G 1 INCH NEEDLE

    FDA Adverse Event
    Malfunction ·COVIDIEN / CARDINAL HEALTH 200, LLC·Product code FMI·November 13, 2018

    MEDLINX SURGICAL MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDEBAR XL

    FDA 510(k)
    FDA Unclassified ·Unknown

    NATURALYTE

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

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 6, 2012

    SUPER POLIGRIP

    FDA Adverse Event
    Injury ·GLAXO SMITHKLINE·Product code KOL·August 27, 2010

    SAFETY NEEDLE 25 X 1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 11, 2018

    SAFETY NEEDLE 25 X 1

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 11, 2018

    SAFETY NEEDLE 25 G X 1"

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMI·December 3, 2018