BEUDAMED
    13 results · 22ms · Sources: EU EUDAMED, US FDA

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    RIVA STAR SILVER DIAMINE FLUORIDE

    FDA Adverse Event
    Injury ·SDI LIMITED·Product code LBH·February 13, 2019

    Riva Star

    FDA 510(k)
    FDA Class 2 ·Dental

    Impact Dome

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215057749·

    LCI OPTION FOR INNOCOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MHI-TM2000 LINEAR ACCELERATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    AQUILEX FLUID CONTROL SYSTEM

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·March 12, 2020

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

    COROX OTW-S 85-BP

    FDA Adverse Event
    Death ·BIOTRONIK SE & CO. KG·Product code NKE·July 15, 2011

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 17, 2008

    FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 30, 2022

    FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 30, 2022

    BLACK SILICONE FILIFORM DOUBLE PIGTAIL URETERAL STENT

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·January 31, 2023

    FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·January 2, 2020