BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    SmarTooth

    FDA 510(k)
    FDA Class 2 ·Dental

    Philips

    FDA UDI
    Sbo Hearing A/S·05714464033188·HearLink 7030 FW 1.1.0

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694022200·FPS Laminar Spreader Assembly

    I.T.S. EXTREMITY FIXATION SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JSA REPROCESSED COMPRESSION SLEEVE DEVICES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 10, 2015

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 4, 2014

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 1, 2011

    PASSPORT V MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC·Product code MHX·July 12, 2013