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

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    LEGIONELLA IMMUNOFLUORESCENT ANTIBODY TEST KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209107834·KIT, PATROL VEHICLE

    The Entasis Dual-Lead Sacroiliac Implant

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SC CERAMIC BALL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN MENTOR GEL IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 29, 2021

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·June 5, 2014

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·October 4, 2010

    SYMBIQ SINGLE CHANNE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA, LTD·Product code FRN·November 12, 2012

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015