BEUDAMED
    9 results · 60ms · Sources: EU EUDAMED, US FDA

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    STARCLOSE SE VASCULAR CLOSURE SYSEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·May 8, 2009

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Injury ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 24, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Injury ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 26, 2021

    IMPELLA 5.5 WITH SMARTASSIST S2 SET, US

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 17, 2026

    PUMP 371 14F LT CMR SET

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·February 18, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code PYX·March 10, 2026

    ZOOM REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·IMPERATIVE CARE. INC·Product code NRY·October 12, 2023

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·April 20, 2010

    DAVINCI XI

    FDA Adverse Event
    Death ·INTUITIVE SURGICAL, INC·Product code NAY·May 27, 2023