BEUDAMED
    8,351 results · 30ms · Sources: EU EUDAMED, US FDA

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    PERCUFLEX PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FAD·December 12, 2022

    KIT, PTFE, INTRODUCER KIT 1-PACK, 6FR

    FDA Adverse Event
    Malfunction ·GREATBATCH MEDICAL·Product code DYB·February 8, 2022

    PADPRO

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code MKJ·December 22, 2025

    LIFEPAK® 20E DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·January 6, 2020

    BARD® INLAY® URETERAL STENT WITH HYDROGLIDE¿ GUIDEWIRE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FAD·March 3, 2025

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 17, 2008

    UNKNOWN

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 17, 2008

    UNKNOWN

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 17, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 17, 2008

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·March 17, 2008

    LADARVISION 4000 LASER

    FDA Adverse Event
    Injury ·ALCON - ORLANDO TECHNOLOGY CENTER·Product code LZS·August 5, 2009

    LADARVISION 4000 LASER

    FDA Adverse Event
    Injury ·ALCON - ORLANDO TECHNOLOGY CENTER·Product code LZS·August 5, 2009

    LADARVISION 4000 LASER

    FDA Adverse Event
    Injury ·ALCON - ORLANDO TECHNOLOGY CENTER·Product code LZS·August 5, 2009

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·November 28, 2023

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·August 21, 2019

    ABSOLUTE .035 SELF EXPANDING STENT SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT VASCULAR INTERVENTION·Product code FGE·September 30, 2004

    SAFE-T-J ROSEN CATHETER EXCHANGE WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DXQ·August 13, 2015

    HEARTSTART MRX

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 28, 2019

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 3, 2019

    HEART START XL

    FDA Adverse Event
    Injury ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 28, 2020