BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    ENVOY PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Stainless Steel Femoral Retrograde and Ankle Arthrodesis Nailing System

    FDA UDI
    ORTHOFIX SRL·18033509851100·REVISION LOCKING SCREW STERILE THREAD D 8 MM L...

    CALCIUM/LITHIUM TEST BECKMAN SYNCHRON EL-ISE ANALY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    RIONET HEARING AID HB-75

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    TALENT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 4, 2018

    SEE H10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·June 4, 2018