BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    MOBILE LEAD PLASTIC X-RAY BARRIERS

    FDA 510(k)
    FDA Class 1 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517377241·CoRoent® LO, 8x10x40mm 5°

    ABC 2 SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    iTClamp50

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMMULITE 2000 TOTAL T3

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CDP·November 7, 2016

    SYSTEM 6 PRECISION HANDPIECE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·June 5, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·November 29, 2012

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 17, 2015