BEUDAMED
    14 results · 30ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code HWC·October 10, 2018

    9616240-2006-00341

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    9616240-2006-00332

    FDA Adverse Event
    Other ·Product code FII·June 1, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    9616240-2006-00339

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    9616240-2006-00340

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    9616240-2006-00350

    FDA Adverse Event
    Malfunction ·Product code FII·June 23, 2006

    9616240-2006-00345

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    GORE TAG THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·April 2, 2010

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEATLTHCARE CORP·Product code LLZ·February 26, 2013

    SUPER POLIGRIP

    FDA Adverse Event
    Other ·GLAXOSMITHKLINE·Product code KOL·February 17, 2011

    U0707 ARENA MACHINE 2 PUMPSWITH NIBP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code KDI·February 15, 2008