BEUDAMED
    50 results · 32ms · Sources: EU EUDAMED, US FDA

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    BITECH BIPOLAR SCISSORS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    C & B FORMULA

    FDA UDI
    AMERICAN TOOTH INDUSTRIES·D772ATI400420770·C & B FORMULA 1 LB SHADE 77

    NAMILON POWDER

    FDA UDI
    AMERICAN TOOTH INDUSTRIES·D772ATI200420770·NAMILON POWDER 16 OZ SHADE 77

    IMMULITE RUBELLA IGM,LKRM1, LKRM2, IMMULITE 2000 RUBELLA IGM, MODEL L2KRM2, L2KRM6

    FDA 510(k)
    FDA Class 2 ·Microbiology

    GLUCANPRO CREAM

    FDA 510(k)
    FDA Unclassified ·Unknown

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY, INC.·Product code LFL·December 12, 2005

    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

    EXCEED ABT RINGLOC-X SHELL

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

    M2A MOD HD COCR DIA28/+3MM T1

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

    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

    ANGIO-SEAL DEVICE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·April 3, 2013

    DEXTRUS 4136

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

    VITALITY DS VR

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

    RECAP SHELL COCR PC DIA56/50MM

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