BEUDAMED
    13 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·July 19, 2021

    AMPLIA MRI CRT-D SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NIK·November 23, 2020

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·June 27, 2019

    CAPSUREFIX NOVUS LEAD MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 27, 2019

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2013

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 10, 2013

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·June 8, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·June 10, 2015

    EVERA MRI XT DR SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LWS·June 27, 2019

    EON

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·January 28, 2014

    E360 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENT·Product code CBK·September 28, 2012

    VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC IRELAND LTD.·Product code MAF·July 25, 2010

    MYOCARDIAL LEAD

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·March 2, 2023