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

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    BURTON KERATOMETER - MODLE 2040

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    ALGINATE FIBER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BUTTON REPLACEMENT GASTROSTOMY DEVICE

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

    REDUCTION FORCEPS WITH POINTS SPEED LOCK 205MM

    FDA Adverse Event
    Malfunction ·SYNTHES TUTTLINGEN·Product code HTD·May 5, 2014

    CORDLESS DRIVER 3

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HRX·January 22, 2013

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·December 10, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 5, 2014