BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    FORTAGEN ORAL MEMBRANE

    FDA 510(k)
    FDA Class 2 ·Dental

    CONMED

    FDA UDI
    Conmed Corporation·10845854005668·OSCILLATOR BLADE, 33 X 71 X 1.2 MM (.047")

    NA

    FDA UDI
    STERILMED, INC.·10888551020909·SAW BLADE OSCILLATING LARGE BONE

    STEREOTAXIS NIOBE MAGNETIC NAVIGATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURESAMPLE-WALLACE ENDOMETRIAL SAMPLER, ENDO 26

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

    NA

    FDA Adverse Event
    Malfunction ·STRYKER SUSTAINABILITY SOLUTIONS LAKELAND·Product code NUJ·April 22, 2013

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·April 15, 2011

    I-FLOW

    FDA Adverse Event
    Injury ·I-FLOW·Product code MEB·July 9, 2008

    BIOLOX HEAD HIP IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·April 25, 2019

    UNKNOWN BIOLOX HEAD

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·February 13, 2018

    CERASUL, HEAD, M/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·November 4, 2019