BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Bovie J-Plasma Precise FLEX Handpiece

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

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776177478·AUVARD VAGINAL SPECULUM . LONG

    INBODY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ABL837 FLEX ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S1 RM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·December 19, 2019

    GYNECARE GYNEMESH* PS

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTO·June 14, 2013

    GEM PREMIER 4000

    FDA Adverse Event
    Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code MZV·June 22, 2011

    LS CLAVE PORT EXT 7"

    FDA Adverse Event
    Malfunction ·HOSPIRA DE COSTA RICA LTD.·Product code FPA·September 15, 2008

    ARTOURA BREAST TISSUE EXPANDER

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·August 21, 2023