BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·May 6, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 13, 2010

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·December 19, 2012

    NEXGEN STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JWH·November 3, 2017

    ARTICULAR SURFACE WITH HINGE POST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 27, 2020

    NEXGEN LONG OFFSET STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·May 16, 2016