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

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    Filters FDA Adverse Event ×

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·March 13, 2017

    VICTORY XL SR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·April 25, 2016

    VICTORY XL DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·May 11, 2017

    ACCENT DR RF

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·November 19, 2015

    ACCENT DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWP·September 7, 2018

    ACCENT DR RF

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·March 31, 2017

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·May 6, 2014

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·October 13, 2010

    ASAHI CONFIANZA PRO PTCA GUIDE WIRE

    FDA Adverse Event
    Injury ·AV-ASAHI·Product code DQX·December 19, 2012

    WAVEONE GOLD PRIMARY 6-FILE STER 25MM

    FDA Adverse Event
    Malfunction ·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EKS·October 6, 2025

    CARPENTIER-EDWARDS SUPRAANNULAR BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·April 24, 2020