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

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    PROPOXPHENE EIA TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    XLIF

    FDA UDI
    Nuvasive, Inc.·00887517417213·XLIF Annulus Cutter, 4x14mm Angled

    Hill-Rom Wireless Connectivity Module

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HL 188 & HL 189 BODY FAT METER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·January 30, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 2, 2011

    RECAP PF FMRL HD RESURF 48MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KXA·July 18, 2014

    TM-ECOCHGTRODE

    FDA Adverse Event
    Other ·NATUS MEDICAL INC·Product code GXY·January 9, 2009