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

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    GLUCOLET AUTOMATIC LANCING DEVICE FOR OBT. BLOOD

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

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690128816·Revision Fluted Offset Stem 20mm x 100mm x 4mm

    PHILIPS UV-A SOLARIUM TYPE HP 3016-SUNLAMP

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

    R PAK

    FDA 510(k)
    FDA Unclassified ·Unknown

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 9, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 6, 2010

    OT SELECT SIMPLE METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 3, 2012