BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    MECHANICAL CHANGE IN IN-VITRO MICRO DEVICE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SPECTRA GUIDEWIRE INTRODUCER NEEDLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Novidia Flowable Composite

    FDA 510(k)
    FDA Class 2 ·Dental

    OT VERIO PRO PLUS METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 19, 2014

    2.4 SL 8 HOLE, X PLATE

    FDA Adverse Event
    BIOMET MICROFIXATION·Product code HWC·October 26, 2010

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·December 20, 2012