BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    TYMPANOSTOMY TUBE

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

    ZOOMCAM LD-10 INTRAORAL CAMERA AND ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·Dental

    OC-Light S FIT

    FDA 510(k)
    FDA Class 2 ·Hematology

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    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·June 24, 2014

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS INC.·Product code LZG·January 21, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·December 31, 2010

    5.0MM TI SIDE-OPENING SCREW 40MM

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNI·June 5, 2012

    5.0MM TI SIDE-OPENING SCREW 40MM

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNI·June 5, 2012

    TI NUT 11MM WIDTH ACROSS FLATS

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNI·June 5, 2012

    TI NUT 11MM WIDTH ACROSS FLATS

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNI·June 5, 2012

    12MM/130 DEG TI CANN TFNA 170MM - STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE: SYNTHES USA PRODUCTS LLC·Product code HSB·January 17, 2018

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 6, 2017