BEUDAMED
    9 results · 26ms · 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 ×

    PSP C & B TEMP

    FDA 510(k)
    FDA Class 2 ·Dental

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707031147·WEB 1ST MOL BANDS W/G8325-03 KIT UL

    Legacy™ GPS® Abutment

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307111269·

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209115297·KIT, SIRK GEN 2 w' CHITOGAUZE XR2

    MEDCOMP VASCU-SHEATH II

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ally Uterine Positioning System

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·October 5, 2010

    ABBOTT M2000SP

    FDA Adverse Event
    Injury ·ABBOTT MOLECULAR, INC.·Product code JQW·July 16, 2012

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2014