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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    HEMOSITE TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    FLEX GOLD

    FDA 510(k)
    FDA Class 1 ·Dental

    BENGAL STACKABLE CAGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ROOT CANAL INSTRUMENT

    FDA Adverse Event
    Other ·MICRO-MEGA SA·Product code EKS·January 25, 2010

    TI CERVICAL SPINE LOCKING PLATE/SMALL STATURE 40MM(32MM)

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code KWQ·February 22, 2013

    PULSE GEN MODEL 103

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·January 18, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·August 1, 2014