BEUDAMED
    49 results · 63ms · Sources: EU EUDAMED, US FDA

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    NEEDLELESS INJECTION SITE MASTER ADAPTER

    FDA Adverse Event
    Injury ·CRITICAL DEVICE CORP.·Product code FOZ·May 16, 1997

    NIMA

    FDA Adverse Event
    Malfunction ·CRITICAL DEVICE CORP.·Product code FPA·July 7, 1998

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 31, 2011

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 16, 2007

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 16, 2007

    R SERIES DEBRIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MED CTR·Product code MKJ·September 27, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 3, 2013

    MODEL 754

    FDA Adverse Event
    Malfunction ·IMPACT PRODUCTS·Product code CBK·June 22, 2015

    UNI-VENT MODEL 731

    FDA Adverse Event
    Malfunction ·IMPACT PRODUCTS·Product code CBK·May 27, 2015

    SPEEDBAND SUPERVIEW SUPER 7 MULTIPLE BAND LIGATOR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MND·October 30, 2009

    OMNIPOD

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code FRN·December 26, 2018

    PROTEGE EVERFLEX SELF-EXPANDING STENT SYSTEM STANDARD

    FDA Adverse Event
    Death ·COVIDIEN·Product code FGE·June 24, 2016

    MITROFLOW DLA

    FDA Adverse Event
    LIVANOVA CANADA CORP·Product code LWR·May 26, 2020

    MITROFLOW LXA

    FDA Adverse Event
    Injury ·LIVANOVA CANADA CORP·Product code LWR·May 15, 2018

    MITROFLOW DLA

    FDA Adverse Event
    Injury ·LIVANOVA CANADA CORP·Product code LWR·May 26, 2020

    BIOPSY FORCEPS

    FDA Adverse Event
    Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·August 11, 2021

    EXTENSION ENGAGE

    FDA Adverse Event
    Injury ·STRYKER CORP. / VOCERA COMMUNICATIONS, INC.·Product code MSX·March 8, 2024

    CROWN PRT PERICARDIAL HEART VALVE

    FDA Adverse Event
    Injury ·LIVANOVA CANADA CORP·Product code LWR·December 3, 2018

    ANIMAS

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·March 23, 2010

    EVIS EXERA II GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·August 11, 2021