BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    Ellipse Supplemental Instrument Trays

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837089160·

    MCCARTNEY ACCESS TUBE

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

    POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BIODESIGN OTOLOGIC REPAIR GRAFT

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code KHJ·January 11, 2018

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 8, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code LWP·June 7, 2013

    ITST FIXATION COMPRESSION RETAINER

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code LXH·June 24, 2011

    ENDOSKELETON® TCS NO 6 SWIVEL DRIVER

    FDA Adverse Event
    Malfunction ·TITAN SPINE, LLC·Product code HXX·January 28, 2016