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

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    INTUITIVE SURGICAL DA VINCI ENDOSCOPIC INSTRUMENT CONTROL SYSTEM AND ENDOSCOPIC INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HairCheck-DT (THC)

    FDA UDI
    Quest Diagnostics·00868586000247·HairCheck-DT (THC) is an ELISA test kit used fo...

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257124574·15-20 MV FOR MEN CLSC CALF STD GREY VII

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690199663·Modular Knee Stem Pilot 23mm x 75mm

    ELECSYS HCG+B CALCHECK

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    ARTICULEZE M HEAD 36MM +15.5

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code JDI·April 8, 2013

    ONE TOUCH ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·May 7, 2008

    DREAMTOME RX SPHINCTEROTOME

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNS·April 5, 2011

    RECAP SHELL COCR PC DIA56/50MM

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