BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    CHANGE IN STERILIZATION PROCEDURE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Vivid iq

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIOSPONGE RECONSTRUCTION DISCS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CURRENT RF DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·April 30, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code LFR·June 26, 2007

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 11, 2012

    GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R and T2 K-Wire Recon, Stryker Trauma GmbH, Prof.-Kuntscher-Strasse 1-5, Schonkirchen, Germany 24232; T2 K-Wire, Sterile R Intended for the temporary stabilization of bone segments or fragments

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·December 28, 2016