BEUDAMED
    6 results · 22ms · 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 ×

    CLINICAL SPECULAR MICROSCOPE, MODEL HAI CL-1000XYZ

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    FASTLOK (STAPLE AND BUCKLE) FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PCI MODEL 2041-A TELEMETRY MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    QUAD BLOOD PACK 500ML WITH FLEXEXCEL RED CELL

    FDA Adverse Event
    Malfunction ·FENWAL·Product code KSR·March 1, 2013

    VERSAFITCUP ACETABULAR SHELL

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL, SA·Product code MEH·January 14, 2011

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·August 8, 2014