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

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    ALL TERRAIN AMIGO

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209109654·

    SUPER SHEATH INTRODUCER SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Winch Kyphoplasty(15 and 20 mm) 11 Gauge Balloon Catheters

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 5, 2014

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 4, 2010

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·November 26, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021