BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    DIRECTFLOW ARTERIAL CANNULA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FULLY AUTOMATIC ELECTRONC BLOOD PRESSURE MONITOR, MODEL KD-5903, KD-5909

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURGICAL MICROSCOPE SYSTEM ORBEYE with IR

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALINITY I CEA REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code DHX·May 18, 2026

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·March 5, 2013

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014