BEUDAMED
    13 results · 43ms · 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

    HS1 DEFIBRILLATOR, FRENCH, EXCHANGE

    FDA Adverse Event
    Malfunction ·PHILIPS NORTH AMERICA LLC·Product code MKJ·February 21, 2023

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 10, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    ENDOSTAT II ELECTROSURGICAL UNIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·September 12, 2008

    TISSUE HEART VALVE

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

    TX1 TISSUE REMOVAL SYSTEM - CONSOLE

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

    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