BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ON-X PROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·ON-X LIFE TEHCNOLOGIES, INC.·Product code DYE·January 14, 2016

    ONX AORTIC ANATOMIC EXT 27/29

    FDA Adverse Event
    Injury ·ONX LIFE TECHNOLOGIES, INC.·Product code LWQ·March 14, 2017

    ONX AORTIC ANATOMIC EXT 23

    FDA Adverse Event
    Injury ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·August 26, 2020

    6000037-1999-00024

    FDA Adverse Event
    Injury ·December 29, 1999

    6000037-1999-00026

    FDA Adverse Event
    Injury ·December 29, 1999

    6000037-1999-00023

    FDA Adverse Event
    Injury ·December 29, 1999

    STEM: AMISTEM-P COLLARED LAT SIZE2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 11, 2020

    BX VELOCITY BILIARY SDS

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code MAF·February 14, 2008

    SMR CEMENTED STEM Ø18 MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWT·November 7, 2023

    ICAST COVERED STENT SYSTEM, 5MMX22MMX120CM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code PRL·April 25, 2025

    ICAST COVERED STENT SYSTEM, 6MMX22MMX120CM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code PRL·April 28, 2025