BEUDAMED
    9 results · 29ms · Sources: EU EUDAMED, US FDA

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    F&P Optiflow Junior 2/2+ Nasal Cannula Interface Range

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AUTOMATED IN VITRO QUANTITATIVE ASSAY FOR THE MEASUREMENT OF ALLERGEN SPECIFIC IGE ANTIBODIES

    FDA 510(k)
    FDA Class 2 ·Immunology

    SURFACE ELECTRODE FOR ELECTROENCEPHALOGRAPHY

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACCU-CHEK ® INSIGHT FLEX

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE, INC.·Product code FPA·October 4, 2018

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·September 6, 2019

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 20, 2015

    TRI-LOCK BPS SZ 3 HI OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. - 1818910·Product code KWA·November 3, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 24, 2011

    TAXUS? LIBERTÉ?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 12, 2013