BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    Oniris

    FDA 510(k)
    FDA Class 2 ·Dental

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171029090·PESSARY, OVAL #7, W/SUPPORT, 3.5”

    FORMATK MAGMA PLATFORM LASER

    FDA Adverse Event
    Injury ·FORMATK SYSTEMS LTD.·Product code GEX·December 19, 2019

    VIBERECT PENILE VIBRATORY STIMULATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    O2PAK OXYGEN GENERATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FORMATK MAGMA PLATFORM

    FDA Adverse Event
    Malfunction ·FOMATK SYSTEMS, LTD·Product code GEX·January 8, 2020

    MERSILENE POLYESTER FIBER MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·June 6, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 6, 2011

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008