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

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    JEE FRAME (VENTILATOR CIRCUIT SUPPORT)

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209116157·

    MERETE DUOTHREADTM BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (1) plus Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (2), A.I.M. Lead Loop Suturing Device plus Tension Assist/Suture Cutter Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    SYMBIQ DUALCHAN INF

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 12, 2014

    UNKNOWN RIGHT REJUVENATE STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·November 20, 2012

    ACTIVA PC

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·September 29, 2010