BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    DAI-R

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO EBI XFIX VISION FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ESSURE

    FDA Adverse Event
    Injury ·CONCEPTUS·Product code HHS·April 15, 2013

    INSIGNIA

    FDA Adverse Event
    Malfunction ·GUIDANT CLONMEL IRELAND·Product code NVZ·April 15, 2011

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 17, 2008

    MERSILENE POLYESTER FIBER MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 23, 2019

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 23, 2019

    PERCLOSE¿ PROSTYLE¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·October 18, 2023

    PERCLOSE¿ PROSTYLE¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code MGB·October 18, 2023

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·May 7, 2021

    MERSILENE POLYESTER FIBER MESH

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·May 15, 2026

    PROLENE POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·May 15, 2026