BEUDAMED
    6 results · 22ms · 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.

    CENTRALITE BACKPOINTER

    FDA 510(k)
    FDA Class 1 ·Radiology

    Summit DuoFix HA Coating

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SSD-203 ULTRASONIC SCANNER

    FDA 510(k)
    FDA Class 2 ·Radiology

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·November 3, 2010

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GDW·February 11, 2014

    PUMP MMT-722NAS PRDGM INS V2.2 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code OYC·November 5, 2007