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

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    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 17, 2019

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·January 24, 2019

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·January 20, 2016

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·July 26, 2018

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·February 27, 2025

    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

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 24, 2013

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·April 6, 2011

    PROXIMATE ILS CURVED CIR STAPL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GDW·July 17, 2008

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·October 8, 2019

    NEU_INTERSTIM_INS

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·July 12, 2012