BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    Stryker Orthopaedics Hip Devices Labeling Update

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PreXion3D Explorer PRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    Precision TC2, Precision TC3, Precision TC4, SEG 100, SEG 150, SEG200

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

    BD ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH LUER ADAPTER

    FDA Adverse Event
    Injury ·BECTON, DICKINSON & CO., (BD)·Product code JKA·January 26, 2018

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code FGE·November 24, 2008

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·July 29, 2011

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 23, 2013