BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    MEDIFIX INC.

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BARD PERMAFIX FIXATION SYSTEM, MODEL 0113012, 0113014, 0113016, 0116018

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

    MeDioStar

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

    MINI QA+ #0 ETH OS-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HWC·May 9, 2018

    TOTAL ASR ACET IMP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·March 7, 2013

    CAPSURE SP NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    SPRINT

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014