BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    HLT 406

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Patient Contoured Implant-PEEK (PCI-PEEK)

    FDA 510(k)
    FDA Class 2 ·Neurology

    ELECSYS PROBNP IMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TRANSVENOUS LEAD

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 9, 2013

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·January 6, 2011

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 22, 2014

    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