BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    NEUROTUBE

    FDA 510(k)
    FDA Class 2 ·Neurology

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983007·posteriors; shade A1; size S; lower jaw

    Skipjack

    FDA UDI
    Seaspine Orthopedics Corporation·10889981138875·MP Wrench

    5983007

    FDA Adverse Event
    Malfunction ·September 28, 2016

    EliA SmDP Immunoassay

    FDA 510(k)
    FDA Class 2 ·Immunology

    PROWICK

    FDA 510(k)
    FDA Unclassified ·Unknown

    ARCHITECT CREATINE KINASE

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018

    ARCHITECT CREATINE KINASE

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018

    ARCHITECT CREATINE KINASE

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018

    GYNECARE GYNEMESH* PS

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTO·February 28, 2013

    LIGASURE ATLAS

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GEI·July 18, 2014

    UNKNOWN DEPUY 28MM +0 HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·February 7, 2011