BEUDAMED
    10 results · 37ms · Sources: EU EUDAMED, US FDA

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    MYSPINE PEDICLE SCREW PLACEMENT GUIDES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MYSPINE STANDARD DRILL GUIDE T07

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MNI·May 10, 2019

    TORNIER BIOFIBER SCAFFOLD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VITEK 2 GRAM NEGATIVE GATIFLOXACIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PELVISOFT ACELLULAR COLLAGEN BIOMESH

    FDA Adverse Event
    Injury ·TISSUE SCIENCE LABORATORIES·Product code FTM·May 16, 2013

    DERMABOND 2

    FDA Adverse Event
    Injury ·ETHICON·Product code MPN·June 17, 2011

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·August 19, 2008

    COREVALVE SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC CORONARY AND STRUCTURAL HEART·Product code NPT·April 24, 2017

    UNKNOWN HIP FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·September 5, 2019

    UNKNOWN HIP ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·September 5, 2019