BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    SUPER-DENT INTERMEDIATE RESTORATIVE MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNCHRON CREATINE KINASE REAGENT

    FDA Adverse Event
    BECKMAN COULTER INC.·Product code CGS·June 17, 2011

    Embrace

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPEEDER 1.5T WRIST ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    DATASCOPE MR MONITOR

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP./PT MONITORING DIVISION·Product code MHX·January 23, 2003

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·February 21, 2013

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 1, 2014

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·January 19, 2011