BEUDAMED
    16 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    P150048

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·September 23, 2024

    P150048

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·September 26, 2025

    TISSUE HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·September 11, 2020

    SEE. H10.

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·December 1, 2020

    REPLACEMENT HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·November 13, 2020

    REPLACEMENT HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·May 29, 2019

    SEE H11

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·February 27, 2025

    EDWARDS PERICARDIAL AORTIC BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·September 27, 2024

    COBAS® EGFR MUTATION TEST V2 P150044

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·April 1, 2026

    COBAS® EGFR MUTATION TEST V2 P150044

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·April 15, 2026

    COBAS® EGFR MUTATION TEST V2 P150044

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·March 27, 2025

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 7, 2014

    TRAPEASE FILTER

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DQO·June 6, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011

    BD CONNECTA STOPCOCK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·December 23, 2020

    TX1 TISSUE REMOVAL SYSTEM - CONSOLE

    FDA Adverse Event
    Malfunction ·AOI, INC·Product code LFL·December 30, 2013