BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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 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

    BLAZER II

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC DP TECHNOLOGIES·Product code LPB·October 10, 2007

    PINN MAR +4 10D 32IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 17, 2013

    ENDEAVOR RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·December 3, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 8, 2014

    HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·March 5, 2019