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

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    Filters Regulation: Us FDA ×

    Affera Integrated Mapping System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Disposable Iris Retract

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114346·FLEXIBLE IRIS RETRACTORS 5 PKS of 5

    DentMix VPS Impression Material

    FDA 510(k)
    FDA Class 2 ·Dental

    Grosz Warming Liquid, Grosz Play Tingling, Grosz KY Yours & Mine

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

    BD NANO¿ ULTRA-FINE¿ PEN NEEDLES 32G X 4MM (90 COUNT)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·August 18, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 23, 2024

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 9, 2023

    BIOSYN UD 4/0 18 P-13

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAM·November 11, 2014

    ANTIMICROBIAL PICC KIT 1-LUMEN: 4.5 FR X

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code LJS·August 24, 2011

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·July 23, 2013