BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    HyPHo Laser System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BRACHYTHERAPY NEEDLES, RP SLEEVE, RP BRACHY-SPACER, GOLD MAKERS

    FDA 510(k)
    FDA Class 2 ·Radiology

    DELUXE NEBULIZER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PENUMBRA MAX PUMP - INDIGO SYSTEM

    FDA Adverse Event
    Malfunction ·PENUMBRA INC., USA·Product code NRY·August 23, 2018

    PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·March 8, 2018

    PENUMBRA SYSTEM ASPIRATION PUMP MAX 220

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·April 9, 2018

    ADVIA CENTAUR

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·June 11, 2013

    MAXI MOVE

    FDA Adverse Event
    Injury ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·July 4, 2011

    WINGED INFUSION SET WITH INJECTION SITE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD)·Product code FMI·September 10, 2008

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·November 18, 2025