BEUDAMED
    7 results · 21ms · 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.

    MUCOUS SPECIMEN TRAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AUSAM TOTAL ALBUMIN ASSAY

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    UltraPrint-Dental Temp C&B UV

    FDA 510(k)
    FDA Class 2 ·Dental

    INCEPTA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 14, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 12, 2010

    TRELLIS 8 120X30

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KRA·July 3, 2014

    CONCERTO NYLON

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·July 27, 2020