BEUDAMED
    1,262 results · 24ms · Sources: EU EUDAMED, US FDA

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    HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ophthalmic Scissors

    FDA UDI
    KATENA PRODUCTS, INC.·00841668105207·HOLLAND DALK SICISSORS LEFT

    COLOR BUFFED (CB) DDH FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RETROGRADE CARDIOPLEGIA CANNULA, SELF-INFLATING, WITH MALLEABLE OR GUIDEWIRE STYLET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 8, 2019

    NUCLEUS CI512 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·June 4, 2019

    HEART START XL

    FDA Adverse Event
    Injury ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 2, 2013

    INSIGNIA PLUS

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code DXY·May 8, 2008

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·April 6, 2011

    BI-MENTUM PLUS CUP 53

    FDA Adverse Event
    Injury ·S.E.R.F SOCIETE DETUDES RECHERCHE FABRICATION·Product code MEH·January 24, 2025

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·September 4, 2019

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·November 27, 2018

    FREEMIE PUMP

    FDA Adverse Event
    Malfunction ·DAO HEALTH·Product code HGX·March 2, 2019

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·January 8, 2019

    NUCLEUS CI532 COCHLEAR IMPLANT WITH SLIM MODIOLAR ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·July 3, 2019

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·September 4, 2019

    NUCLEUS CI532 COCHLEAR IMPLANT WITH SLIM MODIOLAR ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·July 3, 2019

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·December 28, 2020

    BIA400 IMPLANT 4MM W ABUTMENT 14MM

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·June 13, 2019

    NUCLEUS CI522 COCHLEAR IMPLANT WITH SLIM STRAIGHT ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·September 4, 2019