BEUDAMED
    7 results · 28ms · Sources: EU EUDAMED, US FDA

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    CENTRE-DRIVE DRILL-FREE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    AR_N Type Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    IMPAX SE SIGMACOM CLIENT (PACS WORKSTATION)

    FDA 510(k)
    FDA Class 2 ·Radiology

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·August 5, 2015

    UNK JUVEDERM VOLUMA

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·June 30, 2014

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 21, 2013