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

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    Edge Air Digital Flat Panel X-ray Detector

    FDA 510(k)
    FDA Class 2 ·Radiology

    BLOODSTOP HEMOSTATIC GAUZE; IX HEMOSTATIC GAUZE

    FDA 510(k)
    FDA Unclassified ·Unknown

    ADVIA CENTAUR TOXOPLASMA IGG (TOXO G)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 12, 2018

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·January 28, 2019

    PACIFIC XTREME PTA BALLOON CATHETER

    FDA Adverse Event
    Injury ·INVATEC INNOVATIVE TECHNOLOGIES SPA.·Product code LIT·July 20, 2011

    ITREL 3

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 17, 2013

    ALARIS GEMINI INFUSION SYSTEM

    FDA Adverse Event
    Other ·CARDINAL HEALTH ALARIS PRODUCTS·Product code FRN·September 10, 2008

    STEM: AMISTEM C CEMENTED STD SIZE 2

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 19, 2019

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·February 22, 2019