BEUDAMED
    12 results · 28ms · Sources: EU EUDAMED, US FDA

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    Nerve Wrap (07-DW-001-TAB)

    FDA 510(k)
    FDA Class 2 ·Neurology

    MLKJ

    FDA UDI
    Weifang Mingliang Electronics Co., Ltd.·06974077940023·

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112823·BARRON VACUUM PUNCH 9.25MM

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707040743·DB BRACKETS 22 T+7 A+5 CEN U/L

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295122838·TOTAL KNEE REV REAMER 13mm

    ZOE FLUID STATUS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ESOPHYX2 HD

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

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·July 30, 2015

    ESOPHYX Z

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 11, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013