BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    MICRUS MICROCOIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Up&Up

    FDA UDI
    TARGET CORPORATION·06945397906204·Hot+Cold Gel Bead Compress - up & up

    ATLANTIS SR PLUS CORONARY IMAGING CATHETER, MODEL 35975

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LEICA COLPOSCOPE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ADVISOR VITAL SIGNS MONITOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL PM, INC.·Product code CCK·December 24, 2008

    ADVISOR VITAL SIGNS MONITOR

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL PM, INC·Product code DQK·April 28, 2010

    HELICAL BLADE COUPLING SCREW

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code LXH·April 22, 2013

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·April 14, 2011

    CERALAS

    FDA Adverse Event
    Other ·BIOLITEC, INC.·Product code GEX·July 3, 2008

    KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILE

    FDA 510(k)
    FDA Class 2 ·Neurology