BEUDAMED
    4 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    GLIDEWELL HT IMPLANT Ø5.0 X 8 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT·Product code DZE·September 11, 2025

    IMMULITE 2000 OMMA (CA125)

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS LTD.·Product code LTK·November 6, 2008

    HUT EXT DR FINAL ASSY-REVERSE

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code KQS·August 16, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·July 17, 2013