BEUDAMED
    7 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    R3 36MM ID US CRMC LINER 54

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·December 2, 2015

    RESURFACING FEMORAL HEAD 50MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDI·February 28, 2018

    UNKNOWN DEPUY 30MM 3 POSTED OVAL PATELLA

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·April 2, 2013

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·March 25, 2011

    ONE TOUCH BASIC ENHANCED METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·April 14, 2008

    CABLE TENSIONER

    FDA Adverse Event
    Malfunction ·RTI SURGICAL·Product code LXH·December 9, 2021

    BD ANGIOCATH¿ IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·March 19, 2018