BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    WATERLESS SEAL & VACUUM REGULATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HAMMER PAD

    FDA UDI
    Biomet Orthopedics, LLC·00887868048012·

    EBV-VCA IGG ELISA TEST, MODEL EBG-100

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NIRVANA A PERSONAL LUBRICANT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·May 1, 2014

    TI MATRIX LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·November 6, 2012

    SOLARA 3G DEMO 3 LOW SHEAR RECLINE/20 IN H MATRX PB BACK

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·June 5, 2015

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·August 18, 2011

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·August 18, 2011

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·December 19, 2012

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·December 19, 2012