BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ID NOW COVID-19 2.0 TEST KIT 24T (EUA)

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 14, 2024

    ID NOW COVID-19 2.0 TEST KIT 24T (EUA)

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QWR·June 28, 2024

    ID NOW COVID-19 2.0 TEST KIT 24T (EUA)

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QWR·June 28, 2024

    ID NOW COVID-19 2.0 TEST KIT 24T (EUA)

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QWR·June 28, 2024

    AMS ELEVATE PC ANTERIOR PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS (MN)·Product code OTP·May 20, 2014

    SCREW

    FDA Adverse Event
    Injury ·Product code HWC·October 17, 2012

    NONE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·August 31, 2010