BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    IOSERT LENS IMPLANT INSTRUMENT

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209126866·

    Picasso Pro Diode Laser (002-00460)

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

    JAKOBI SURG. INSTR- #11 38/39/45/46/67

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NIM CONTACT®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·June 6, 2014

    IFUSE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·SI-BONE·Product code OUR·November 29, 2012

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DRY·September 3, 2010