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

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    REVERE STABILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Affiniti™ PC

    FDA UDI
    TORNIER, INC.·00846832003006·

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814237·GENUMEDI PT SILVER L VI

    CODMAN DISPOSABLE PERFORATOR, MODEL(S) 26-1222, 26-1223

    FDA 510(k)
    FDA Class 2 ·Neurology

    ALTUS MEDICAL FAMILY OF COOLGLIDE LASERS, MODELS COOLGLIDE I, COOLGLIDE II, AND FUTURE MODELS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DUAL INCU I

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 22, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

    SYNCHRON LX® I 725 CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·June 13, 2011

    LINOX TD 65/16

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH AND CO.·Product code LWS·August 8, 2008