BEUDAMED
    688 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    O-F II ACET SHELL 48MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDI·April 17, 2018

    ILET BIONIC PANCREAS

    FDA Adverse Event
    Injury ·BETA BIONICS, INC.·Product code QFG·April 6, 2026

    BD U F II 3/10CC 31G SYRINGE

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMF·October 31, 2008

    BD U-F II 1CC 31G INSULIN SYRINGE

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMF·September 15, 2008

    BD U-F II 3/10CC 31G INSULIN SYRINGE

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMF·February 8, 2008

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·March 26, 2014

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·January 2, 2014

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·April 2, 2024

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·January 3, 2019

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LNQ·December 27, 2018

    PROXIMATE*PPH PROCEDURE SET

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 17, 2019

    FROVA INTUBATING INTRODUCER

    FDA Adverse Event
    Injury ·COOK INC·Product code LRC·March 8, 2021

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·April 19, 2018

    2008 MACHINE

    FDA Adverse Event
    Injury ·Product code FII·April 3, 2014

    GAMBRO

    FDA Adverse Event
    Injury ·GAMBRO RENAL PRODUCTS·Product code FII·March 11, 2004

    FRESENIUS 2008H

    FDA Adverse Event
    Injury ·FRESENIUS USA·Product code FII·January 27, 2004

    FRESENIUS DIALYSIS MACHINE

    FDA Adverse Event
    Injury ·FRESENIUS·Product code FII·April 16, 2010

    FRESENIUS

    FDA Adverse Event
    Injury ·FRESENIUS USA·Product code FII·July 2, 1996

    BAXTER 550

    FDA Adverse Event
    Injury ·*·Product code FII·July 2, 1996

    BAXTER

    FDA Adverse Event
    Injury ·*·Product code FII·July 2, 1996