BEUDAMED
    6 results · 19ms · 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 ×

    VISTA FINOFF TRANSILLUMINATOR (AC-POWERED)

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Deep Learning Image Reconstruction

    FDA 510(k)
    FDA Class 2 ·Radiology

    ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 25, 2014

    PRODISC-L REVISIONS

    FDA Adverse Event
    Injury ·SYNTHES·Product code MJO·January 2, 2013

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·November 8, 2010