BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    SPECTACLE FRAMES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    UNIMARK HOME PREGNANCY TEST DEVICE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TI STAR IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·December 20, 2010

    GII

    FDA Adverse Event
    Injury ·SMITH&NEPHEW, INC·Product code JWH·July 14, 2014

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 31, 2012