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

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    Filters FDA Adverse Event ×

    GORE VIABAHN ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code NIP·September 4, 2020

    GORE VIABAHN VBX BALLOON EXPANDABLE ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code PRL·September 4, 2020

    GORE VIABAHN ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code NIP·September 4, 2020

    GORE VIABAHN VBX BALLOON EXPANDABLE ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code PRL·September 4, 2020

    VERTECOR MIDLINE CEMENT STAGING OSTEOTOME

    FDA Adverse Event
    Malfunction ·DFINE INC.·Product code GFI·April 14, 2015

    CLOSED SYSTEM TRANSFER DEVICE PHASEAL PROTECTOR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code ONB·July 17, 2025

    ATRAAUCLIP

    FDA Adverse Event
    Death ·SPK TECHNOLOGY, INC.·Product code GDO·January 30, 1995

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    INTEGRITY AFK DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 15, 2014

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    POWERLED 300+DFK

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 8, 2020

    D 860 - CFK - POLYMER

    FDA Adverse Event
    Malfunction ·BERCHTOLD GMBH & CO. KG·Product code GDC·February 16, 2017

    D 860 - CFK - POLYMER

    FDA Adverse Event
    Injury ·BERCHTOLD GMBH & CO. KG·Product code GDC·March 23, 2020

    IVENIX INFUSION SYSTEM

    FDA Adverse Event
    Malfunction ·FRESENIUS KABI USA LLC·Product code FPA·March 27, 2025