BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    URO PRO

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LEFORTE SYSTEM BONE PLATE & SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·February 4, 2016

    PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 1, 2015

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 5, 2014

    FIXODENT ADHESIVE CREAM, VERSION UNKNOWN

    FDA Adverse Event
    Other ·PROCTER & GAMBLE MFG. GMBH·Product code KOO·April 30, 2013

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 28, 2011

    KOH-EFFICIENT,ARCH,4.0CM

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code LKF·April 27, 2016