BEUDAMED
    7 results · 28ms · Sources: EU EUDAMED, US FDA

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    BICON BONE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X200MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·November 7, 2012

    DIAZYME LP(A) ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    Reprocessed Response Diagnostic Electrophysiology Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NSEAL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·February 28, 2013

    UNICEL® DXI 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code LFX·February 9, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2014