BEUDAMED
    11 results · 25ms · Sources: EU EUDAMED, US FDA

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    LIFEPAK 9 DEFIBRILLATOR & CARDIAC MONITOR/MODIFIED

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VuePoint

    FDA UDI
    Nuvasive, Inc.·00887517180384·VuePoint Screw, 3.5x10mm Fav Angle MA

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·10840117400372·

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·00840117408654·

    Duo Lumbar Interbody Fusion Device

    FDA UDI
    SPINEOLOGY INC.·M7402905510·Duo, Non-Lordotic, 55 x 10mm

    4905510

    FDA Adverse Event
    Death ·July 10, 2015

    ENZYMATIC THEOPHYLLINE REAGENT, #500-82

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PERTAC-HYBRID

    FDA 510(k)
    FDA Class 2 ·Dental

    CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 28, 2014

    FLEXTEND

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·January 9, 2013

    HYLAMER 10D 56 OR 68ODX28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDL·November 19, 2010