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

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    ENDOLAP RESECTOSCOPE CUTTING LOOP ELECTRODE

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

    Duo Ti Expandable Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7402974516·Duo Ti, 45 x 16mm, 15°

    9 FRENCH LITHOTRIPTER ELECTRODE, MODIFICATION

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

    MODEL V4 AUDIOMETER

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    ZONA PLUS

    FDA Adverse Event
    Injury ·ZONA HEALTH·Product code BXB·March 25, 2013

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 28, 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