BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    IMMULITE CK-MB, CATALOG # LKCP1 (100 TESTS), LKCP5 (500 TESTS)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981495·anteriors; shade BL3; mould BS2

    Republic Spine Dark Star Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CELL-DYN EMERALD SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    CELL-DYN EMERALD CLEANER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·April 20, 2016

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 27, 2013

    PREMIUM SURGICLIP S-9.0 TITANIUM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC PUERTO RICO, INC.·Product code FZP·July 25, 2014

    X-STOP IPD SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·February 8, 2011