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

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    IMMUSTRIP(TM) SM ELISA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·10888867127194·.045" GUIDE WIRE TROCAR TIP

    Arthrex

    FDA UDI
    Provision·B504OMAR8737410·

    Reprocessed ArthoCare Ablation Wand

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ADVANCE EMIT-AED PRIMEDONE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ANTHREX GUIDE WIRE; 1.1MM AR 8737-41

    FDA Adverse Event
    Malfunction ·ANTHREX, INC.·Product code HWC·August 23, 2021

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 19, 2010

    ENERGEN

    FDA Adverse Event
    Death ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·December 14, 2012

    2.15MM X 22MM SPIRAL ROUTER

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·November 27, 2013