BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·July 11, 2011

    CANNULA, EGRESS, 3.0MM

    FDA Adverse Event
    Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HRX·January 4, 2013

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 8, 2013

    MEDFUSION 3500 SYRINGE INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD·Product code FRN·February 17, 2011

    *

    FDA Adverse Event
    Malfunction ·*·Product code KDI·December 19, 2007

    CANNULA, EGRESS, 3.0MM

    FDA Adverse Event
    Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HRX·January 4, 2013

    HEARTMATE 3 SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·May 22, 2023

    CANNULA, EGRESS, 3.0MM

    FDA Adverse Event
    Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HRX·June 11, 2012

    PRIMEADVANCED

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code LGW·July 22, 2016

    CANNULA, EGRESS, 3.0MM

    FDA Adverse Event
    Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code HRX·February 6, 2013

    KIT SHORT STEM FLEX 2-1/4

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HHW·February 22, 2021

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·February 3, 2025

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·February 3, 2025