BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    MICOMED - HALM ZIELKE INSTRUMENTATION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982006·posteriors; shade A1; size S; upper jaw

    AMS SPECTRA CONCEALABLE PENILE PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Omni Hysteroscope, Omni Hysteroscope Kits, Omni Sheaths

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

    SMART PERFUSION PACK: APEX MBR FMC/MID WEST REG LEXINGTON, KY

    FDA Adverse Event
    Injury ·Product code DTZ·September 11, 2007

    OT DELICA LANCING DEVICE

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 28, 2013

    CRYOMAZE

    FDA Adverse Event
    Malfunction ·ATS MEDICAL, INC.·Product code OCL·January 7, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014