BEUDAMED
    3 results · 35ms · 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 FDA Adverse Event ×

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·September 1, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·November 18, 2014

    2.9MM TI MATRIXRIB LCKNG SCREWSELF-TAPPING/10MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 1, 2013