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

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    MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION

    FDA 510(k)
    FDA Class 2 ·Neurology

    CT LUCIA

    FDA UDI
    CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100720·3-piece, monofocal, hydrophobic, acrylic, intra...

    DETACH 18 AND DETACH 11, NEUROLOGICAL EMBOLIZATION COIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    AT HOME DRUG TEST, MODEL 9133 T

    FDA 510(k)
    FDA Unclassified ·Unknown

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·March 14, 2013

    CURRENT RF DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

    GENESIS II

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. ORTHOPEDIC DIVISION-GERMANY·Product code JWH·April 12, 2011

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012