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

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    LOQTEQ DISTAL DORSOLATERAL HUMERUS PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEUROLASE, MODELS 150V, 150C, 1064

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    KERATOR

    FDA 510(k)
    FDA Class 2 ·Dental

    MYSPINE STANDARD DRILL GUIDE T07

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

    PROLENE POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·May 29, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 17, 2011

    ARCHITECT C8000

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