BEUDAMED
    56 results · 23ms · Sources: EU EUDAMED, US FDA

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    OLSEN MEDICAL ANTERIOR CERVICAL VERTEBRAE PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PAIN CARE 3000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OLYMPUS SPRAY CATHETER PW-6C-1

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    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

    SOFPORT ADVANCED OPTIC LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code HQL·April 3, 2013

    DEXTRUS 4135

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG.·Product code NVZ·March 29, 2011

    VITALITY 2 DR

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008