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

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    SPEC MODEL M-31

    FDA 510(k)
    FDA Class 2 ·Radiology

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776362843·Potts Elevator,

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036028992·

    FIXATION STYLETS, MODELS 335-287 AND 335-288

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DISPOSABLE STORAGE CAP

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

    WAVEWRITER ALPHA 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 11, 2024

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 17, 2024

    BD VACUTAINER® URINE COLLECTION STRAW

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·November 7, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 1, 2017

    BD VACUTAINER® PLUS PLASTIC TRANSPORT KIT FOR UA CHEMISTRY URINE TESTING

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·November 27, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 5, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 5, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 1, 2017

    BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 1, 2017

    120 ML BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code KDT·December 1, 2017

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·May 2, 2013

    LIFEPAK EXPRESS(R) DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·September 15, 2014

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 16, 2011