BEUDAMED
    17 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNK_SMART TOUCH BIDIRECTIONAL SF

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·November 17, 2021

    NEOBLUE

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·September 1, 2017

    NEOBLUE 3

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·August 17, 2017

    ULTRA SAFE HANDLE, STUBBY

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·June 5, 2019

    NEOBLUE

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·August 28, 2017

    NEOBLUE 3

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·September 13, 2017

    NEOBLUE 3

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·September 14, 2017

    NEOBLUE 3

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·August 11, 2017

    DOLPHIN STD WTR RESIST HD

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·June 5, 2019

    EEA 28MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL·Product code GDW·March 6, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 25, 2011

    BOSTON SCIENTIFIC

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code DXT·February 20, 2008

    RUSCH TRUMR SET: HDL+ MIL 1,2,3 MAC 2,3,4

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·June 30, 2019

    NEOBLUE 3

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·July 21, 2017

    NEOBLUE 3 LED PHOTOTHERAPY SYSTEM

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·June 30, 2017

    NEOBLUE 3 LED PHOTOTHERAPY SYSTEM

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·July 27, 2017

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·December 2, 2008