BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    LYSUS INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HP+

    FDA UDI
    TEKNIMED·03760177043091·

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K0604250·Tray, Base, 4.25"

    ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER

    FDA 510(k)
    FDA Class 2 ·Neurology

    S57D DIGITAL OPERATING ROOM CAMERA

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SIEMENS : ARTISTE MV

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code IYE·July 30, 2010

    DESARA BLUE TV

    FDA Adverse Event
    Injury ·CALDERA MEDICAL INC.·Product code OTN·December 5, 2019

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 25, 2013

    SYNCHRON® CX5 DELTA CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·April 16, 2011

    ENDO GIA UNIVERSAL 12MM SINGLE USE INST

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·June 12, 2008