BEUDAMED
    8 results · 30ms · Sources: EU EUDAMED, US FDA

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    NASAL CANNULA

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    FARRORS TMJ CASSETTE HOLDER

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SURGICAL MEDICAL DEVICE CAUTERY

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 28, 2014

    AUTOSONIX ULTRA SHEARS 5MM INSTRUMENT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURG·Product code LFL·October 8, 2012

    CXD II

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 2, 2010

    Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 16o, LEFT, FOR CEMENTED USE ONLY, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-06-22, b) 41, 44, 47, 50 head, Medium, Item Number 314-06-23, c) 44, 47, 50, 53 head, Large, Item Number 314-06-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-06-25; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024

    OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 9800 MD Motorized C-arm System, 892.1650 Image-intensified fluoroscopic x-ray system. The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The system includes features specifically designed for use in diagnostic and interventional cardiac imaging procedures and is also intended for cholangiography, endoscopic, urologic orthopedic, neurologic, vascular, critical care and emergency room procedures. It may be used for other imaging applications at the physician's discretion.

    FDA Enforcement
    Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012