BEUDAMED
    6 results · 21ms · 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 ×

    Avenger Radial Head System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SBI FOOT AND ANKLE CANNULATED SCREW SYSTEM, MODEL 100-0061

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IVENT101

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·June 27, 2013

    XIA II TORQUE WRENCH

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code LXH·July 20, 2011

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·October 21, 2014