BEUDAMED
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    EM-X

    FDA 510(k)
    FDA Class 2 ·Hematology

    PED FOLYSIL CATH 1.5ML CH06/5

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code EZL·February 1, 2016

    HEARTSTART MRX-EMX DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 15, 2010

    EMX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·January 15, 2013

    EMX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·April 3, 2013

    HEARTSTART MRX-EMX DEFIBRILLATOR

    FDA Adverse Event
    Death ·PHILIPS HEALTHCARE·Product code MKJ·January 6, 2011

    HEARTSTART MRX-EMX DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·February 14, 2011

    HEARTSTART MRX- EMX DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·March 20, 2009

    HEARTSTART MRX-EMX DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILLIPS HEALTHCARE·Product code MKJ·February 6, 2009

    EMX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 13, 2013

    HEARTSTART MRX -EMX DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 12, 2015

    HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·November 28, 2017

    RAPID RHINO 550 EPISTAXIS DEVICE

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code EMX·March 13, 2012

    4.5 CM ANTERIOR, EPISTAXIS

    FDA Adverse Event
    Injury ·ARTHROCARE CORP.·Product code EMX·April 1, 2010

    NOZ-STOP

    FDA Adverse Event
    Injury ·PERRY SMITH & NEPHEW MEDICAL·Product code EMX·July 9, 1996

    RAPID RHINO 5.5 CM

    FDA Adverse Event
    Injury ·APPLIED THERAPEUTICS, BHK HOLDING·Product code EMX·March 11, 2004

    RAPID RHINO 5.5 CM

    FDA Adverse Event
    Injury ·APPLIED THERAPEUTICS, BHK HOLDING·Product code EMX·March 11, 2004

    7.5CM ANTERIOR/POSTERIOR

    FDA Adverse Event
    Injury ·ARTHROCARE CORP.·Product code EMX·April 27, 2021

    EPISTAXIS CATHETER

    FDA Adverse Event
    Death ·SMITHS MEDICAL INC.·Product code EMX·December 1, 2014

    7.5 ANTERIOR/POSTERIOR

    FDA Adverse Event
    Malfunction ·ARTHROCARE UK LTD·Product code EMX·April 19, 2007