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

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    Dornier MINNOW Ureteral Catheter

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

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776175719·SOPHER OVUM FCP . JAW

    PATCH, PLEDGET AND INTRACARDIAC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRACE DYNAMIC TORP

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 21, 2025

    OPTIBOND XTR

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code KLE·June 26, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 25, 2011

    OMNI

    FDA Adverse Event
    HOSPIRA GLOBAL MEDICAL AFFAIRS·Product code FRN·August 14, 2008

    SUBDURAL ELECTRODE

    FDA Adverse Event
    Malfunction ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GYC·August 18, 2025