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

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    Lumipulse G Progesterone-N Calibrators

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    VERSANT VALUE

    FDA UDI
    FGX INTERNATIONAL INC.·00193033308035·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111288005·TC IRIS SCISS CVD SERR S/S 4.5

    AYCAN WORKSTATION OSIRIX PRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    INSUFLOW DEVICE, MODEL 6198

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

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 10, 2024

    SUNRISE ECLYPSIS

    FDA Adverse Event
    Injury ·ALLSCRIPTS·Product code NSX·July 9, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code ITI·June 11, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Death ·CORDIS DE MEXICO·Product code NIQ·September 17, 2008

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015