BEUDAMED
    6 results · 23ms · 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 ×

    HUMIDIFIER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FHT (FECAL HEME TEST)

    FDA 510(k)
    FDA Class 2 ·Hematology

    DTX AND DTX PLUS DISPOSABLE PRESSURE TRANSDUCERS AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TA PREMIUM 90-4.8 TITANIUM DLU

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY USSC·Product code GDW·February 1, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FNL·December 27, 2010

    OT VERIO PRO PLUS METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 21, 2014