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

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    THERAPEUTIC APPARATUS, DIERKER TYPE

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

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515199415·Blount Single Prong Retr, 37mm blade, 10 1/2"

    PROLIXUS TOTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO: OCU-FILM TIP COVER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 18, 2014

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 25, 2007

    GYNECARE MORCELLEX* TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·October 3, 2012