BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    WASTON General Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131281883·NERA2, MINIBTE 312 WL 85 SIL

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171027782·PESSARY, CUBE #2, W/O DRAINS, 33mm

    CELLTRACKS AUTOPREP SYSTEM MODEL:9541

    FDA 510(k)
    FDA Class 1 ·Hematology

    ATLANTIS PV

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020

    STR RINGLOC+ BTN LTCH INSERTER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LXH·June 6, 2013

    TI 3-D HEAD FOR TI CLICK'X SCREWS

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code MNI·June 24, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014