BEUDAMED
    6 results · 18ms · 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 ×

    APEXIT ROOT CANAL SEALER

    FDA 510(k)
    FDA Class 2 ·Dental

    CONTROL TM 8

    FDA 510(k)
    FDA Class 2 ·Hematology

    SMART-READ EZTEST-STEAM SCBI AND TEST PACK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 7, 2015

    CATALYS PRECISION LASER SYSTEM

    FDA Adverse Event
    Injury ·OPTIMEDICA CORPORATION·Product code OOE·June 12, 2014

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC·Product code FNL·October 29, 2010