BEUDAMED
    435 results · 23ms · 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 ×

    MARK III PHASED ARRAY SHOULDER COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    POSTERIOR DISTAL TIBIA PLATE , RIGHT

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665024869·

    Specials

    FDA UDI
    Seaspine Orthopedics Corporation·10889981182540·Trial, 20x15x9mm, 7 deg. Lordosis, w/o Stops

    MX8000 IDT CT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    HP M2376A DEVICE LINK SYSTEM, MODEL M2376A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON MANUFACTURING, LTD. / HUNTINGTON·Product code MFK·November 23, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON MANUFACTURING, LTD. / HUNTINGTON·Product code MFK·November 4, 2009

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD. / HUNTINGTON·Product code MFK·November 23, 2009

    OPTI-FREE REPLENISH

    FDA Adverse Event
    Injury ·ALCON - FORTH WORTH/ALCON LABORATORIES INC.·Product code LPN·June 24, 2009

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·November 4, 2009

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL·Product code GDW·April 2, 2013

    INTELECT TRANSPORT COMO

    FDA Adverse Event
    Injury ·DJ ORTHOPEDICS DE MEXICO·Product code IMG·March 31, 2011

    VITALITY DS

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    GEMINI ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH ALARIS PRODUCTS·Product code FPA·June 4, 2009

    LFL INSTRUMENT, ULTRASONIC SURGICAL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code LFL·May 4, 2009

    GIA 80-3.8 SINGLE USE RELOADABLE STAPLER

    FDA Adverse Event
    Injury ·PONCE - USS·Product code GDW·May 4, 2009

    ACCU-CHEK ACTIVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 12, 2009

    ALARIS SMARTSITE BLOOD ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH ALARIS PRODUCTS·Product code BRZ·March 5, 2009

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·November 4, 2009

    CLEAN CUFFS, KIT (WRIST AND ANKLE SET)

    FDA Adverse Event
    Malfunction ·POSEY, S. DE R. L. DE C.V.·Product code FMQ·November 11, 2009