BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    FIX-C PEEK ACIF SA System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OGYILI TENS/NMES Stimulator

    FDA 510(k)
    FDA Class 2 ·Neurology

    breastscape v1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·October 4, 2022

    IMPLANT, ENDOSSEOUS, ORTHODONTIC

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code OAT·November 14, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 9, 2011

    PINN CAN BONE SCREW 6.5MMX25MM

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code NDJ·July 29, 2013