BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    400um Perforator and Accessory Vein Ablation Kit

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

    N/A

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327616286·Spine Guidance 5 Sales Demo

    REJUVENATE MODULAR HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RETRIEVE IMPLANT CEMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS

    FDA Adverse Event
    Injury ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 20, 2013

    PLUM XLM W/MODIFD B

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 7, 2011

    VITROS 5, 1 FS CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·September 29, 2008