BEUDAMED
    13 results · 22ms · 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

    DEPUY ASR XL FEM IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·June 4, 2014

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 29, 2012

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 27, 2010

    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

    OXYSEPT

    FDA Adverse Event
    Injury ·AMO(HANGZHOU) CO., LTD.·Product code LPN·June 5, 2023

    SEE H11

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

    CONSEPT 1 STEP LL

    FDA Adverse Event
    Injury ·AMO(HANGZHOU) CO., LTD.·Product code LPN·August 28, 2023

    EDWARDS PERICARDIAL AORTIC BIOPROSTHESIS

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