BEUDAMED
    6 results · 20ms · 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 ×

    KAVO INTRASEPT 905

    FDA 510(k)
    FDA Class 1 ·Dental

    DISCRETE PHOTOMETRIC CHEMISTRY ANALYSER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BURTON SLIT LAMP - MODEL 850

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HUDSON ADULT CONVENTIONAL BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAI·January 23, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 4, 2014

    ULTRAFLEX ESOPHAGEAL STENT SYSTEM, ULTRAFLEX DIAMONDBILIARY STENT SYSTEM, ULTRAF

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code JCT·December 21, 2010