BEUDAMED
    4 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 9, 2022

    MULTI-LINK CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·March 26, 2013

    RENAISSANCE 26

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·March 10, 2011

    HOSPIRA PLUM A + INFUSION PUMP

    FDA Adverse Event
    Injury ·HOSPIRA AND CO.·Product code FRN·March 20, 2008