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

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    LIQUICHEK ELEVATED CRP CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MODIFICATION TO: DATEX-OHMEDA CARDIOCAP 5 (REV B) AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIS ENGINE

    FDA 510(k)
    FDA Class 2 ·Neurology

    36MM COCR BIOMET FEM HD STD NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 13, 2016

    UNKNOWN EXCEED HIP

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·August 5, 2016

    UNKNOWN RECAP 48MM HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·September 16, 2016

    36MM 12/14 TPR FEM HEAD -4 NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 28, 2016

    EXCEED ABT M2A-36 MOD HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 28, 2016

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 7, 2011

    EXCEED ABT RINGLOC-X SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·July 20, 2017

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 5, 2012

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 31, 2012

    M2A MOD HD COCR DIA28/+3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·December 23, 2015

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 29, 2012

    32MM COCR BIOMET FEM HD STD NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·February 16, 2016

    RECAP/MAGNUM ACETABULAR SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·February 15, 2017

    EXCEED ABT M2A-36 MOD HEAD -3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·June 1, 2016

    LIBERTY CYCLER SET, SINGLE CONN./ EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code FKX·April 4, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 30, 2011

    CONTAK RENEWAL 3

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008