BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    INSTRUMENT DETERGENT CONCENTRATE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SeaSpine Spacer System - Pacifica

    FDA UDI
    Seaspine Orthopedics Corporation·10889981088224·Slap Hammer Connector, Small

    BIOPURE HX2 REVERSE OSMOSIS WATER PURIFICATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ULTIMATE PROFESSIONAL CONTINUOUS FLOW COLONIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    1933149-1997-00005

    FDA Adverse Event
    Injury ·PURITAN-BENNETT CORP/SLEEP THERAPEUTICS DIVISION·Product code BZA·November 12, 1997

    COBAS 8000 C702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CFR·January 29, 2013

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIVISION·Product code INK·December 13, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 14, 2014