BEUDAMED
    7 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 ×

    ESPE(R) -SIL

    FDA 510(k)
    FDA Class 2 ·Dental

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909139652·REVELATION DIAMOND 889-008F - 5 PACK

    STATPAL BLOOD GAS MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BeautiBond Xtreme

    FDA 510(k)
    FDA Class 2 ·Dental

    UNKNOWN DEPUY CORAIL STEM

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code JDI·January 14, 2013

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC·Product code LZG·November 19, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 3, 2014