BEUDAMED
    6 results · 26ms · 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.

    OPUS PSA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    PULSE RATE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CYTOQUANT HNFS CELLS

    FDA 510(k)
    FDA Class 1 ·Hematology

    OXIMAX N-560 PULUSE OXIMETER

    FDA Adverse Event
    Malfunction ·MEDIANA·Product code DPZ·May 30, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011