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

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    KENDALL-LTP DISPOSABLE TEMPERATURE PROBES (DTP1,DTP2,DTP3,DTP4)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PANOVIEW

    FDA UDI
    Richard Wolf GmbH·04055207023266·NEPHROSCOPE 12° 20.8FR WL 224MM rigid, with pa...

    CELL-DYN

    FDA UDI
    ABBOTT LABORATORIES·00380740021085·ENZYM CLNR 2X50 ML

    HCL LABORATORY SYSTEMS 200 -LISA-

    FDA Adverse Event
    Other ·HYCEL DIAGNOSTICS·Product code JJF·November 8, 2000

    PLURIMUS CARDIAC EVALUATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BATTERY-POWERED TOOTHBRUSH

    FDA 510(k)
    FDA Class 1 ·Dental

    VIRTUOSO DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 15, 2013

    SYNCHRON LX 20 PRO CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·January 19, 2011

    OXFORD UNI FEMORAL LG

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·July 29, 2014