BEUDAMED
    10 results · 24ms · Sources: EU EUDAMED, US FDA

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    XENON LIGHT SOURCE MODEL 5121

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

    INFX-8000V, V6.20

    FDA 510(k)
    FDA Class 2 ·Radiology

    COVACLEARAG COLLAGEN WITH SILVER ANTIMICROBIAL GEL SHEET DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    TT (TRACHEOSTOMY TUBES)

    FDA Adverse Event
    Malfunction ·Product code BTR·October 24, 2017

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·February 9, 2013

    DIALOG A + HE/BIC

    FDA Adverse Event
    Malfunction ·B. BRAUN AVITUM AG·Product code KDI·July 17, 2014

    VENTAK PRIZM 2

    FDA Adverse Event
    Injury ·GUIDANT CLONMEL IRELAND·Product code LWS·January 7, 2011

    SELDRILL-SCHANZSCR Ø5 L200/80 SST

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018

    SELDRILL-SCHANZSCR Ø5 L200/80 SST

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code KTT·April 12, 2018

    ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020