BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    ROC

    FDA Adverse Event
    Injury ·ALPHATEC SPINE INC.·Product code KWP·March 19, 2009

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013

    2.5MM REAMING ROD WITH BALL TIP/950MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HTO·September 19, 2014

    STERIS

    FDA Adverse Event
    Other ·STERIS COPORATION·Product code MED·May 19, 2011

    VASOPRESS DIGITAL MINI PUMP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code JOW·January 6, 2020

    1-CHANNEL HOLTER MONITOR CARDIOKEY

    FDA Adverse Event
    Injury ·BRAEMAR MANUFACTURING, LLC·Product code MWJ·July 11, 2019

    VASOPRESS DIGITAL MINI PUMP

    FDA Adverse Event
    Malfunction ·COMPRESSION THERAPY CONCEPTS, INC.·Product code JOW·February 18, 2020

    VASOPRESS DIGITAL MINI PUMP

    FDA Adverse Event
    Malfunction ·COMPRESSION THERAPY CONCEPTS, INC.·Product code JOW·September 17, 2019

    VASOPRESS DIGITAL MINI PUMP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code JOW·November 19, 2019

    VASOPRESS DIGITAL MINI PUMP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code JOW·November 19, 2019

    VASOPRESS DIGITAL MINI PUMP

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code JOW·December 10, 2019