BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·April 25, 2023

    MAESTRO FOOT SWITCH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·November 3, 2023

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 7, 2023

    MAESTRO 4000 POD, 100W

    FDA Adverse Event
    Malfunction ·STELLARTECH RESEARCH CORPORATION·Product code LPB·August 17, 2023

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·October 2, 2023

    CORMATRIX ECM FOR CARDIAC TISSUE REPAIR

    FDA Adverse Event
    Injury ·CORMATRIX CARDIOVASCULAR, INC.·Product code DXZ·May 14, 2014

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    KENSTONE METAL·Product code IKX·November 5, 2012

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·August 24, 2010

    PROMETRA REFILL KIT

    FDA Adverse Event
    Injury ·FLOWONIX MEDICAL, INC.·Product code LKK·August 14, 2020

    ADULT ET CLOSED SUCTION CATHETER

    FDA Adverse Event
    Malfunction ·FLEXICARE MEDICAL LTD·Product code BSY·September 23, 2025