BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ACCESSORIES

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code DQX·March 20, 2025

    SYMBIQ DUAL CHANNEL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 1, 2013

    TECNIS CL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·January 26, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 31, 2014

    AIA-900

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·February 24, 2016

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024

    TOSOH AIA-900

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·December 13, 2016

    A1A-600II

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·October 28, 2016

    TOSOH AIA-1800

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·November 11, 2016

    AIA-360

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·March 3, 2016