BEUDAMED
    65 results · 29ms · Sources: EU EUDAMED, US FDA

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    MICROPROTEIN REAGENT SET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496070757·SECRET SKIN, SIZE XS, NATUR, MICRO-MASSAGING PO...

    CABLE,IBP BD,IM2202,12PIN

    FDA UDI
    Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904005324·

    LFIT V40 FEMORAL HEAD COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VARELISA CARDIOLIPIN IGA ANTIBODIES, MODELS 15748 & 15796

    FDA 510(k)
    FDA Class 2 ·Immunology

    ARCOS 18X150MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY 60MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016

    OMNIGUIDE BEAMPATH FIBER AND ADAPTER

    FDA Adverse Event
    OMNIGUIDE, INC.·Product code GEX·October 19, 2010

    ARCOS HA MODULAR REVISION SYSTEM STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 10, 2017

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY / TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 10, 2017

    ENSEAL G2 STRAIGHT JAW

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·April 22, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 14, 2011

    BD PRECISION GLIDE NEEDLE

    FDA Adverse Event
    Other ·BECTON DICKINSON·Product code FMI·July 1, 2008

    ARCOS DISTAL SCREW TI DIA5X50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 12, 2016

    ARCOS DISTAL SCREW TI DIA5X45MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 12, 2016

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY TYPE 1 TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 14, 2017

    ARCOS MODULAR REVISION HIP

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code KWA·February 16, 2017

    ARCOS STS DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 23, 2017

    ARCOS MODULAR REVISION HIP SYSTEM STANDARD BROACH PROXIMAL BODY

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·January 6, 2017

    ARCOS CON SZ A STD 50MM HA 0MM SZ A

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 26, 2021