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

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    Filters Regulation: Us FDA ×

    CHIN WAFER

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

    FLUKE BIOMEDICAL

    FDA registration
    FLUKE BIOMEDICAL·2 products·🇺🇸 United States

    HEMOSORB

    FDA 510(k)
    FDA Unclassified ·Unknown

    BOX PEEK VBR SYSTEM,

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    E1 RINGLOC BIPOLAR 28X51MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·June 17, 2019

    BIOMEX SHELL PC DIA48MM LN 22

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 2, 2015

    HELICAL BLADE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KTT·January 18, 2013

    SCREW-IN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 6, 2014