BEUDAMED
    61 results · 18ms · Sources: EU EUDAMED, US FDA

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    ZOLL E SERIES DEFIBRILLATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981182526·Trial, 20x15x7mm, 7 deg. Lordosis, w/o Stops

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369023·SMOOTH TRAC TRACTION BAR

    SULZER VASCUTEK GELSOFT ERS VASCULAR PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RHS HELMET

    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

    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

    GIA UNIVERSAL

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL·Product code GDW·April 2, 2013

    CAIRE LIBERATOR 60

    FDA Adverse Event
    Injury ·CAIRE, INC.·Product code BYJ·March 31, 2011

    CONTAK RENEWAL 3

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

    RECAP SHELL COCR PC DIA56/50MM

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

    DHS®/DCS® COUPLING SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES JENNERSVILLE·Product code LXH·May 5, 2013