BEUDAMED
    7 results · 38ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Injury ·PHYSIO CONTROL CORP.·Product code MLN·January 17, 1997

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·February 1, 2018

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    AMS SPHINCTER 800 URINARY PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code EZY·March 12, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 1, 2011

    CODMAN BACTISEAL EVD CATHETER

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·October 5, 2018

    CODMAN BACTISEAL EVD CATHETER

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·October 5, 2018