BEUDAMED
    19 results · 24ms · Sources: EU EUDAMED, US FDA

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    SURELIFE ARM BP MONITOR-PREMIUM

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODUCTS, LLC·Product code DXN·June 19, 2018

    BLUNT TIP SCREW, ÿ 4X38MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·October 24, 2024

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·April 13, 2013

    VENTED AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·Product code BTT·July 29, 2020

    PROLIEVE THERMODILITATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 15, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 1, 2013

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 29, 2016

    BLUNT TIP SCREW, ÿ 4X38MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·October 24, 2024

    PROXIMAL HUMERUS, LEFT, ÿ 7X160MM

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HSB·October 8, 2024

    PROXIMAL HUMERUS, RIGHT, LONG, ÿ 8.5X220MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·October 24, 2024

    SINGLE USE GUIDWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code OCY·July 10, 2020

    NEEDLE 25GA 5/8IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·December 7, 2020

    MINICOLLECT TUBE 0.5 ML K2E K2EDTA LAVENDER CAP, WITH CROSS CUT, SPRAY-DRIED

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE GMBH·Product code JKA·August 28, 2020

    NEEDLE 25GA 5/8IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·January 15, 2021

    COBE SPECTRA

    FDA Adverse Event
    Injury ·TERUMO BCT·Product code GKT·April 8, 2022

    COBE SPECTRA

    FDA Adverse Event
    Injury ·TERUMO BCT·Product code GKT·April 8, 2022

    COBE SPECTRA

    FDA Adverse Event
    Injury ·TERUMO BCT·Product code GKT·April 8, 2022

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·September 4, 2009