BEUDAMED
    12 results · 32ms · Sources: EU EUDAMED, US FDA

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    ANGIOSCULPT PTA SCORING BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Channel Drain

    FDA UDI
    C. R. Bard, Inc.·00801741049859·Channel Drain, 19Fr. Round 3/4 Fluted with 4.7m...

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496072225·BE YOU STEP-UP CURVY, SIZE ML-XL, NERO, OPAQUE ...

    Genius Total Knee System

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215021764·

    STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code MHY·October 7, 2024

    OR TABLE/MAGNETOM OPEN VIVA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ATTAIN 6215 VENOGRAM BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 27, 2024

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·July 19, 2007

    VUEPOINT OCT SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code MNI·March 6, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·April 28, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008